id
stringlengths 11
11
| tags
stringlengths 10
777
| text
stringlengths 2
1.5k
| dataset_num
int64 1
3
| tokens
sequence | ner_tags
sequence |
---|---|---|---|---|---|
NCT03145298 | 12:22:cancer, | History of malignancy within the last 5 years | 1 | [
"History",
"of",
"malignancy",
"within",
"the",
"last",
"5",
"years"
] | [
0,
0,
3,
0,
0,
0,
0,
0
] |
NCT02429934 | 22:33:chronic_disease | Subjects with active CNS disease | 1 | [
"Subjects",
"with",
"active",
"CNS",
"disease"
] | [
0,
0,
0,
2,
2
] |
NCT02962557 | 34:63:chronic_disease | Patients with known or suspected obstructive sleep apnea (OSA) | 1 | [
"Patients",
"with",
"known",
"or",
"suspected",
"obstructive",
"sleep",
"apnea",
"(",
"OSA",
")"
] | [
0,
0,
0,
0,
0,
2,
2,
2,
2,
0,
0
] |
NCT02089607 | 1:18:chronic_disease | Innominate artery | 1 | [
"Innominate",
"artery"
] | [
2,
2
] |
NCT01972919 | 36:46:chronic_disease | Patients with and without regional adenopathy are eligible | 1 | [
"Patients",
"with",
"and",
"without",
"regional",
"adenopathy",
"are",
"eligible"
] | [
0,
0,
0,
0,
0,
2,
0,
0
] |
NCT02200445 | 18:48:treatment, | Received another investigational new drug (IND) within 5 half-lives of that agent before the planned commencement of SC IL-2 | 1 | [
"Received",
"another",
"investigational",
"new",
"drug",
"(",
"IND",
")",
"within",
"5",
"half-lives",
"of",
"that",
"agent",
"before",
"the",
"planned",
"commencement",
"of",
"SC",
"IL-2"
] | [
0,
0,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03038620 | 12:31:chronic_disease,33:47:chronic_disease,51:64:chronic_disease | History of gallbladder disease (cholelithiasis or cholecystitis) | 1 | [
"History",
"of",
"gallbladder",
"disease",
"(",
"cholelithiasis",
"or",
"cholecystitis",
")"
] | [
0,
0,
2,
2,
0,
2,
0,
2,
0
] |
NCT01697293 | 102:109:allergy_name,151:161:allergy_name,163:173:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biologic composition to PTX-200 or other agents used in the study (e.g., imidazoles, quinolones) | 1 | [
"History",
"of",
"allergic",
"reactions",
"attributed",
"to",
"compounds",
"of",
"similar",
"chemical",
"or",
"biologic",
"composition",
"to",
"PTX-200",
"or",
"other",
"agents",
"used",
"in",
"the",
"study",
"(",
"e.g.",
",",
"imidazoles",
",",
"quinolones",
")"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
4,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
4,
0,
4,
0
] |
NCT03112603 | 1:8:treatment,20:25:chronic_disease,58:89:treatment,107:127:treatment,131:141:cancer | Steroid refractory cGvHD occurring after a non-scheduled donor lymphocyte infusion (DLI) administered for preemptive treatment of malignancy recurrence | 1 | [
"Steroid",
"refractory",
"cGvHD",
"occurring",
"after",
"a",
"non-scheduled",
"donor",
"lymphocyte",
"infusion",
"(",
"DLI",
")",
"administered",
"for",
"preemptive",
"treatment",
"of",
"malignancy",
"recurrence"
] | [
1,
0,
2,
0,
0,
0,
0,
1,
1,
1,
1,
0,
0,
0,
0,
1,
1,
0,
3,
0
] |
NCT02361554 | 15:37:chronic_disease | Subject has a neurological condition | 1 | [
"Subject",
"has",
"a",
"neurological",
"condition"
] | [
0,
0,
0,
2,
2
] |
NCT01666769 | 23:64:treatment | Supported with either venoarterial (VA) or venovenous (VV) ECMO | 1 | [
"Supported",
"with",
"either",
"venoarterial",
"(",
"VA",
")",
"or",
"venovenous",
"(",
"VV",
")",
"ECMO"
] | [
0,
0,
0,
1,
1,
1,
1,
1,
1,
0,
0,
0,
0
] |
NCT02374021 | 1:16:treatment,,, | MTX monotherapy for ≥ 8 weeks at ≥ 15mg weekly or ≥ 7.5 mg weekly with a documented intolerance to higher doses | 1 | [
"MTX",
"monotherapy",
"for",
"≥",
"8",
"weeks",
"at",
"≥",
"15mg",
"weekly",
"or",
"≥",
"7.5",
"mg",
"weekly",
"with",
"a",
"documented",
"intolerance",
"to",
"higher",
"doses"
] | [
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02188121 | 62:71:treatment,,, | defined as entering one of the two-year First Episode Clinic treatment programs as a de novo patient (new disease) or having been diagnosed >2 years ago and had at least six visits in the past 12 months (prevalent disease) | 1 | [
"defined",
"as",
"entering",
"one",
"of",
"the",
"two-year",
"First",
"Episode",
"Clinic",
"treatment",
"programs",
"as",
"a",
"de",
"novo",
"patient",
"(",
"new",
"disease",
")",
"or",
"having",
"been",
"diagnosed",
">",
"2",
"years",
"ago",
"and",
"had",
"at",
"least",
"six",
"visits",
"in",
"the",
"past",
"12",
"months",
"(",
"prevalent",
"disease",
")"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03059004 | 1:23:chronic_disease | Inflammatory arthritis | 1 | [
"Inflammatory",
"arthritis"
] | [
2,
2
] |
NCT02068092 | 29:49:treatment,58:67:treatment,85:91:cancer | Must not participate in any other clinical trial for the treatment or prevention of cancer unless they are no longer receiving the intervention and are in the follow-up phase only. Participants must also agree not to join such a trial while participating in this study | 1 | [
"Must",
"not",
"participate",
"in",
"any",
"other",
"clinical",
"trial",
"for",
"the",
"treatment",
"or",
"prevention",
"of",
"cancer",
"unless",
"they",
"are",
"no",
"longer",
"receiving",
"the",
"intervention",
"and",
"are",
"in",
"the",
"follow-up",
"phase",
"only",
".",
"Participants",
"must",
"also",
"agree",
"not",
"to",
"join",
"such",
"a",
"trial",
"while",
"participating",
"in",
"this",
"study"
] | [
0,
0,
0,
0,
0,
1,
1,
1,
0,
0,
1,
0,
0,
0,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02309580 | 12:46:treatment,52:66:treatment,68:78:treatment,,122:132:treatment | Concurrent systemic immunosuppressant therapy (eg, cyclosporine A, tacrolimus, etc.) within 28 days of the first dose of study drug | 1 | [
"Concurrent",
"systemic",
"immunosuppressant",
"therapy",
"(",
"eg",
",",
"cyclosporine",
"A",
",",
"tacrolimus",
",",
"etc",
".",
")",
"within",
"28",
"days",
"of",
"the",
"first",
"dose",
"of",
"study",
"drug"
] | [
0,
1,
1,
1,
0,
0,
0,
1,
1,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1
] |
NCT02333162 | 40:48:treatment | Since these patients already had first allo-SCT | 1 | [
"Since",
"these",
"patients",
"already",
"had",
"first",
"allo-SCT"
] | [
0,
0,
0,
0,
0,
0,
1
] |
NCT02128906 | ,,53:65:treatment | Pregnant women are excluded from this study because chemotherapy | 1 | [
"Pregnant",
"women",
"are",
"excluded",
"from",
"this",
"study",
"because",
"chemotherapy"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02844751 | 1:25:treatment, | Corticosteroid injection at treatment site within 1 month | 1 | [
"Corticosteroid",
"injection",
"at",
"treatment",
"site",
"within",
"1",
"month"
] | [
1,
1,
0,
0,
0,
0,
0,
0
] |
NCT01795313 | 28:42:treatment, | Patients may have received re-irradiation but not to the index lesion within 4 weeks | 1 | [
"Patients",
"may",
"have",
"received",
"re-irradiation",
"but",
"not",
"to",
"the",
"index",
"lesion",
"within",
"4",
"weeks"
] | [
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01976429 | 26:38:chronic_disease | syndrome predisposing to otitis media | 1 | [
"syndrome",
"predisposing",
"to",
"otitis",
"media"
] | [
0,
0,
0,
2,
2
] |
NCT02201992 | 108:124:chronic_disease,138:162:chronic_disease,164:188:chronic_disease,203:221:chronic_disease,226:263:chronic_disease | Patients must NOT have uncontrolled intercurrent illness including, but not limited to, serious ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, uncontrolled cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements | 1 | [
"Patients",
"must",
"NOT",
"have",
"uncontrolled",
"intercurrent",
"illness",
"including",
",",
"but",
"not",
"limited",
"to",
",",
"serious",
"ongoing",
"or",
"active",
"infection",
",",
"symptomatic",
"congestive",
"heart",
"failure",
",",
"unstable",
"angina",
"pectoris",
",",
"uncontrolled",
"cardiac",
"arrhythmia",
",",
"or",
"psychiatric",
"illness/social",
"situations",
"that",
"would",
"limit",
"compliance",
"with",
"study",
"requirements"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0,
0,
2,
2,
2,
0,
2,
2,
2,
0,
0,
2,
2,
0,
0,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0
] |
NCT02355002 | 46:51:treatment, | Use of other psychotropic medications (e.g., SSRIs) will be allowed provided the dose has been stable for > 12 weeks | 1 | [
"Use",
"of",
"other",
"psychotropic",
"medications",
"(",
"e.g.",
",",
"SSRIs",
")",
"will",
"be",
"allowed",
"provided",
"the",
"dose",
"has",
"been",
"stable",
"for",
">",
"12",
"weeks"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03011684 | 19:31:treatment | Has not yet begun chemotherapy | 1 | [
"Has",
"not",
"yet",
"begun",
"chemotherapy"
] | [
0,
0,
0,
0,
1
] |
NCT02516696 | ,,,85:92:cancer | Subject has a Karnofsky performance status ≥60% (>50% if due to bony involvement of myeloma (see Appendix IV) | 1 | [
"Subject",
"has",
"a",
"Karnofsky",
"performance",
"status",
"≥60",
"%",
"(",
">",
"50",
"%",
"if",
"due",
"to",
"bony",
"involvement",
"of",
"myeloma",
"(",
"see",
"Appendix",
"IV",
")"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
3,
0,
0,
0,
0,
0
] |
NCT03093272 | 13:40:chronic_disease, | symptomatic peripheral vascular disease within 6 months prior to randomization | 1 | [
"symptomatic",
"peripheral",
"vascular",
"disease",
"within",
"6",
"months",
"prior",
"to",
"randomization"
] | [
0,
2,
2,
2,
0,
0,
0,
0,
0,
0
] |
NCT02016235 | 55:95:chronic_disease,97:112:chronic_disease,,,146:162:chronic_disease,181:199:treatment,201:216:treatment,221:230:treatment, | Exclusion criteria for calcium stone formers include: primary or secondary hyperparathyroidism, hyperthyroidism, estimated GFR <40 ml/mn/1.73m2, chronic diarrhea states; intake of thiazide diuretics, glucocorticoids, or estrogens within one month of the study | 1 | [
"Exclusion",
"criteria",
"for",
"calcium",
"stone",
"formers",
"include",
":",
"primary",
"or",
"secondary",
"hyperparathyroidism",
",",
"hyperthyroidism",
",",
"estimated",
"GFR",
"<",
"40",
"ml/mn/1.73m2",
",",
"chronic",
"diarrhea",
"states",
";",
"intake",
"of",
"thiazide",
"diuretics",
",",
"glucocorticoids",
",",
"or",
"estrogens",
"within",
"one",
"month",
"of",
"the",
"study"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
2,
2,
2,
2,
0,
2,
0,
0,
0,
0,
0,
0,
0,
2,
2,
0,
0,
0,
0,
1,
1,
0,
1,
0,
0,
1,
0,
0,
0,
0,
0,
0
] |
NCT01959698 | 1:19:chronic_disease, | Myocardial infarct within 6 months before enrollment | 1 | [
"Myocardial",
"infarct",
"within",
"6",
"months",
"before",
"enrollment"
] | [
2,
2,
0,
0,
0,
0,
0
] |
NCT01714596 | 100:129:chronic_disease | Patients likely to have severe problems maintaining follow-up, including patients diagnosed with a severe psychiatric conditions, patients who live too far outside the hospital's catchment area | 1 | [
"Patients",
"likely",
"to",
"have",
"severe",
"problems",
"maintaining",
"follow-up",
",",
"including",
"patients",
"diagnosed",
"with",
"a",
"severe",
"psychiatric",
"conditions",
",",
"patients",
"who",
"live",
"too",
"far",
"outside",
"the",
"hospital",
"'s",
"catchment",
"area"
] | [
0,
0,
0,
0,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02382549 | 61:71:treatment, | Participants who have received the following medications or treatments at any time within 4 weeks of registration | 1 | [
"Participants",
"who",
"have",
"received",
"the",
"following",
"medications",
"or",
"treatments",
"at",
"any",
"time",
"within",
"4",
"weeks",
"of",
"registration"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02578732 | 14:22:chronic_disease | Uncontrolled diabetes. If patient has diabetes, confirmation on status (controlled or uncontrolled) required at registration | 1 | [
"Uncontrolled",
"diabetes",
".",
"If",
"patient",
"has",
"diabetes",
",",
"confirmation",
"on",
"status",
"(",
"controlled",
"or",
"uncontrolled",
")",
"required",
"at",
"registration"
] | [
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02579967 | 15:49:chronic_disease,53:83:chronic_disease,109:117:cancer,165:189:chronic_disease | Patients with hemophagocytic lymphohistiocytosis or macrophage activation syndrome related to an underlying lymphoma with no other clinical history suggestive of a primary immunodeficiency | 1 | [
"Patients",
"with",
"hemophagocytic",
"lymphohistiocytosis",
"or",
"macrophage",
"activation",
"syndrome",
"related",
"to",
"an",
"underlying",
"lymphoma",
"with",
"no",
"other",
"clinical",
"history",
"suggestive",
"of",
"a",
"primary",
"immunodeficiency"
] | [
0,
0,
2,
2,
0,
2,
2,
2,
0,
0,
0,
0,
3,
0,
0,
0,
0,
0,
0,
0,
0,
2,
2
] |
NCT02719847 | 10:20:cancer | Patients malignancy is consistent with well differentiated neuroendocrine (carcinoid) histology | 1 | [
"Patients",
"malignancy",
"is",
"consistent",
"with",
"well",
"differentiated",
"neuroendocrine",
"(",
"carcinoid",
")",
"histology"
] | [
0,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02048722 | 1:6:cancer | Tumor deemed unresectable or metastatic | 1 | [
"Tumor",
"deemed",
"unresectable",
"or",
"metastatic"
] | [
3,
0,
0,
0,
0
] |
NCT02324582 | 1:26:treatment, | Prior monoclonal antibody within 4 weeks prior to study | 1 | [
"Prior",
"monoclonal",
"antibody",
"within",
"4",
"weeks",
"prior",
"to",
"study"
] | [
1,
1,
1,
0,
0,
0,
0,
0,
0
] |
NCT01652092 | 14:48:chronic_disease | Other severe Combined Immune Deficiencies (CID) | 1 | [
"Other",
"severe",
"Combined",
"Immune",
"Deficiencies",
"(",
"CID",
")"
] | [
0,
0,
2,
2,
2,
2,
0,
0
] |
NCT02778282 | 21:44:treatment | Seeking to initiate buprenorphine treatment or currently receiving buprenorphine treatment but had recent positive illicit opioid urine toxicology or missed scheduled urine toxicology | 1 | [
"Seeking",
"to",
"initiate",
"buprenorphine",
"treatment",
"or",
"currently",
"receiving",
"buprenorphine",
"treatment",
"but",
"had",
"recent",
"positive",
"illicit",
"opioid",
"urine",
"toxicology",
"or",
"missed",
"scheduled",
"urine",
"toxicology"
] | [
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02514083 | 7:17:cancer | Prior malignancy | 1 | [
"Prior",
"malignancy"
] | [
0,
3
] |
NCT02048852 | 54:66:treatment,68:76:treatment,78:92:treatment,97:112:treatment,121:128:treatment,132:141:treatment | not using an acceptable form of birthcontrol such as Depo-provera, Norplant, tubal ligation and barrier methods such as condoms or diaphragm | 1 | [
"not",
"using",
"an",
"acceptable",
"form",
"of",
"birthcontrol",
"such",
"as",
"Depo-provera",
",",
"Norplant",
",",
"tubal",
"ligation",
"and",
"barrier",
"methods",
"such",
"as",
"condoms",
"or",
"diaphragm"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1,
0,
1,
1,
0,
1,
1,
0,
0,
1,
0,
1
] |
NCT00715611 | 32:47:chronic_disease | Patients with serious unstable medical illness | 1 | [
"Patients",
"with",
"serious",
"unstable",
"medical",
"illness"
] | [
0,
0,
0,
0,
2,
2
] |
NCT01356290 | ,,,,,,,,,,304:313:treatment,319:328:treatment,333:349:treatment | Participants must have normal organ and bone marrow function (ALT <5x institutional upper limit of normal, creatinine <1.5x institutional upper limit of normal for age, WBC >1000/mm3, platelets > 20,000/mm3. Patients with values less than WBC 2000/mm3 or platelets 50,000/mm3 will require initiation of treatment with etoposide and cyclophosphamide at a lower starting dose as defined within the protocol | 1 | [
"Participants",
"must",
"have",
"normal",
"organ",
"and",
"bone",
"marrow",
"function",
"(",
"ALT",
"<",
"5x",
"institutional",
"upper",
"limit",
"of",
"normal",
",",
"creatinine",
"<",
"1.5x",
"institutional",
"upper",
"limit",
"of",
"normal",
"for",
"age",
",",
"WBC",
">",
"1000/mm3",
",",
"platelets",
">",
"20,000/mm3",
".",
"Patients",
"with",
"values",
"less",
"than",
"WBC",
"2000/mm3",
"or",
"platelets",
"50,000/mm3",
"will",
"require",
"initiation",
"of",
"treatment",
"with",
"etoposide",
"and",
"cyclophosphamide",
"at",
"a",
"lower",
"starting",
"dose",
"as",
"defined",
"within",
"the",
"protocol"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03179449 | 27:38:allergy_name | Known hypersensitivity to ferumoxytol or any of its components | 1 | [
"Known",
"hypersensitivity",
"to",
"ferumoxytol",
"or",
"any",
"of",
"its",
"components"
] | [
0,
0,
0,
4,
0,
0,
0,
0,
0
] |
NCT02484404 | ,29:62:treatment | within 6 weeks prior to the first dose of the study treatment are not eligible | 1 | [
"within",
"6",
"weeks",
"prior",
"to",
"the",
"first",
"dose",
"of",
"the",
"study",
"treatment",
"are",
"not",
"eligible"
] | [
0,
0,
0,
0,
0,
0,
1,
1,
1,
1,
1,
1,
0,
0,
0
] |
NCT01360606 | 1:31:treatment,35:62:treatment,72:79:treatment,81:105:treatment,107:124:treatment,126:149:treatment,151:181:treatment,185:197:treatment,287:300:treatment,,390:399:treatment,461:465:treatment,521:537:treatment, | Previous systemic chemotherapy or non-radiation local therapy (such as surgery, hepatic arterial therapy, chemoembolization, radiofrequency ablation, percutaneous ethanol injection or cryoablation) is allowed. The lesion must however have shown criteria of progression based on RECIST. Local therapy must be completed at least 4 weeks prior to the baseline scan. This is to create a safer treatment environment and to help determine the effect of treatment by SBRT alone. Patients will be allowed to go onto appropriate systemic therapy, as determined by their medical oncologist, 2 weeks following delivery of SBRT | 1 | [
"Previous",
"systemic",
"chemotherapy",
"or",
"non-radiation",
"local",
"therapy",
"(",
"such",
"as",
"surgery",
",",
"hepatic",
"arterial",
"therapy",
",",
"chemoembolization",
",",
"radiofrequency",
"ablation",
",",
"percutaneous",
"ethanol",
"injection",
"or",
"cryoablation",
")",
"is",
"allowed",
".",
"The",
"lesion",
"must",
"however",
"have",
"shown",
"criteria",
"of",
"progression",
"based",
"on",
"RECIST",
".",
"Local",
"therapy",
"must",
"be",
"completed",
"at",
"least",
"4",
"weeks",
"prior",
"to",
"the",
"baseline",
"scan",
".",
"This",
"is",
"to",
"create",
"a",
"safer",
"treatment",
"environment",
"and",
"to",
"help",
"determine",
"the",
"effect",
"of",
"treatment",
"by",
"SBRT",
"alone",
".",
"Patients",
"will",
"be",
"allowed",
"to",
"go",
"onto",
"appropriate",
"systemic",
"therapy",
",",
"as",
"determined",
"by",
"their",
"medical",
"oncologist",
",",
"2",
"weeks",
"following",
"delivery",
"of",
"SBRT"
] | [
1,
1,
1,
0,
1,
1,
1,
0,
0,
0,
1,
0,
1,
1,
1,
0,
1,
0,
1,
1,
0,
1,
1,
1,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02143050 | ,,70:79:treatment, | Fertile males should use an effective method of contraception during treatment and for at least 3 months after completion of treatment, as directed by their physician | 1 | [
"Fertile",
"males",
"should",
"use",
"an",
"effective",
"method",
"of",
"contraception",
"during",
"treatment",
"and",
"for",
"at",
"least",
"3",
"months",
"after",
"completion",
"of",
"treatment",
",",
"as",
"directed",
"by",
"their",
"physician"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02514083 | 1:37:treatment,39:51:treatment,53:65:treatment,69:89:treatment | Concomitant immunomodulatory therapy, chemotherapy, radiotherapy or experimental therapy | 1 | [
"Concomitant",
"immunomodulatory",
"therapy",
",",
"chemotherapy",
",",
"radiotherapy",
"or",
"experimental",
"therapy"
] | [
1,
1,
1,
0,
1,
0,
1,
0,
1,
1
] |
NCT02933034 | 12:22:chronic_disease | develop an arrhythmia prior to or during either of the exercise tests; SeeMore should not be administered | 1 | [
"develop",
"an",
"arrhythmia",
"prior",
"to",
"or",
"during",
"either",
"of",
"the",
"exercise",
"tests",
";",
"SeeMore",
"should",
"not",
"be",
"administered"
] | [
0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02423525 | 21:46:cancer,48:79:cancer,81:105:cancer,129:139:cancer,157:166:treatment, | effectively treated non-melanoma skin cancers, carcinoma in situ of the cervix, ductal carcinoma in situ or effectively treated malignancy that has been in remission for more than 3 years and is considered to be cured | 1 | [
"effectively",
"treated",
"non-melanoma",
"skin",
"cancers",
",",
"carcinoma",
"in",
"situ",
"of",
"the",
"cervix",
",",
"ductal",
"carcinoma",
"in",
"situ",
"or",
"effectively",
"treated",
"malignancy",
"that",
"has",
"been",
"in",
"remission",
"for",
"more",
"than",
"3",
"years",
"and",
"is",
"considered",
"to",
"be",
"cured"
] | [
0,
0,
3,
3,
3,
0,
3,
3,
3,
3,
3,
3,
0,
3,
3,
3,
3,
0,
0,
0,
3,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02563678 | 19:37:treatment, | Prior work in the hyperbaric chamber in the last 72 hours | 1 | [
"Prior",
"work",
"in",
"the",
"hyperbaric",
"chamber",
"in",
"the",
"last",
"72",
"hours"
] | [
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0
] |
NCT03114891 | 64:67:treatment,69:79:treatment,81:95:treatment,97:104:treatment | Medication use that substantially reduces seizure threshold to TMS (olanzapine, chlorpromazine, lithium) | 1 | [
"Medication",
"use",
"that",
"substantially",
"reduces",
"seizure",
"threshold",
"to",
"TMS",
"(",
"olanzapine",
",",
"chlorpromazine",
",",
"lithium",
")"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
1,
0,
1,
0,
1,
0
] |
NCT03169543 | 12:28:chronic_disease,30:38:chronic_disease,40:48:chronic_disease,50:67:chronic_disease,69:82:chronic_disease,93:112:chronic_disease | History of bipolar disorder, delirium, dementia, amnestic disorder, schizophrenia and other psychotic disorders | 1 | [
"History",
"of",
"bipolar",
"disorder",
",",
"delirium",
",",
"dementia",
",",
"amnestic",
"disorder",
",",
"schizophrenia",
"and",
"other",
"psychotic",
"disorders"
] | [
0,
0,
2,
2,
0,
2,
0,
2,
0,
2,
2,
0,
2,
0,
0,
2,
2
] |
NCT02053792 | 1:8:treatment | Surgery substudy | 1 | [
"Surgery",
"substudy"
] | [
1,
0
] |
NCT02929069 | 1:4:chronic_disease | HIV-positive status | 1 | [
"HIV-positive",
"status"
] | [
2,
0
] |
NCT02473536 | 28:46:chronic_disease | Subjects with a history of pulmonary embolism is excluded | 1 | [
"Subjects",
"with",
"a",
"history",
"of",
"pulmonary",
"embolism",
"is",
"excluded"
] | [
0,
0,
0,
0,
0,
2,
2,
0,
0
] |
NCT02427997 | 1:11:treatment | medication regime is likely to change during the course of the study | 1 | [
"medication",
"regime",
"is",
"likely",
"to",
"change",
"during",
"the",
"course",
"of",
"the",
"study"
] | [
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02464696 | 22:35:treatment | Contraindications to NIPPV therapy | 1 | [
"Contraindications",
"to",
"NIPPV",
"therapy"
] | [
0,
0,
1,
1
] |
NCT02573493 | 1:19:treatment,21:48:treatment,53:76:treatment,81:86:cancer | Prior chemotherapy, prior EGFR targeted therapy, or prior radiation therapy for HNSCC | 1 | [
"Prior",
"chemotherapy",
",",
"prior",
"EGFR",
"targeted",
"therapy",
",",
"or",
"prior",
"radiation",
"therapy",
"for",
"HNSCC"
] | [
1,
1,
0,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
3
] |
NCT02826343 | 12:38:chronic_disease,41:47:chronic_disease,73:85:chronic_disease | History of myocardial infarction (MI) , stroke and/or poorly controlled hypertension | 1 | [
"History",
"of",
"myocardial",
"infarction",
"(",
"MI",
")",
",",
"stroke",
"and/or",
"poorly",
"controlled",
"hypertension"
] | [
0,
0,
2,
2,
2,
0,
0,
0,
2,
0,
0,
0,
2
] |
NCT02384954 | 5:8:chronic_disease | Not HIV positive | 1 | [
"Not",
"HIV",
"positive"
] | [
0,
2,
0
] |
NCT03188042 | 1:24:chronic_disease,81:89:chronic_disease,91:97:chronic_disease | End-stage organ disease or medical condition with subsequent vision loss (e.g., diabetes, stroke) | 1 | [
"End-stage",
"organ",
"disease",
"or",
"medical",
"condition",
"with",
"subsequent",
"vision",
"loss",
"(",
"e.g.",
",",
"diabetes",
",",
"stroke",
")"
] | [
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2,
0,
2,
0
] |
NCT02494869 | 1:11:chronic_disease | Thrombosis of lower extremities | 1 | [
"Thrombosis",
"of",
"lower",
"extremities"
] | [
2,
0,
0,
0
] |
NCT02344355 | ,102:125:cancer | Patients must have newly diagnosed (i.e., within 5 weeks), histologically or cytologically confirmed glioblastoma multiforme | 1 | [
"Patients",
"must",
"have",
"newly",
"diagnosed",
"(",
"i.e.",
",",
"within",
"5",
"weeks",
")",
",",
"histologically",
"or",
"cytologically",
"confirmed",
"glioblastoma",
"multiforme"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
3,
3
] |
NCT02341963 | 12:20:allergy_name | Allergy to ketamine | 1 | [
"Allergy",
"to",
"ketamine"
] | [
0,
0,
4
] |
NCT02593123 | 1:8:chronic_disease,10:23:chronic_disease,28:44:chronic_disease | Medical, psychological, or social condition that, in the opinion of the investigator, may increase the patient's risk or limit the patient's adherence with study requirements | 1 | [
"Medical",
",",
"psychological",
",",
"or",
"social",
"condition",
"that",
",",
"in",
"the",
"opinion",
"of",
"the",
"investigator",
",",
"may",
"increase",
"the",
"patient",
"'s",
"risk",
"or",
"limit",
"the",
"patient",
"'s",
"adherence",
"with",
"study",
"requirements"
] | [
2,
0,
2,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03169543 | 9:19:chronic_disease | Current depression as assessed on the HDRS-17 (for depressed group only) | 1 | [
"Current",
"depression",
"as",
"assessed",
"on",
"the",
"HDRS-17",
"(",
"for",
"depressed",
"group",
"only",
")"
] | [
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01742299 | ,32:63:treatment,80:92:treatment,,151:160:treatment | Female sterilization (have had surgical bilateral oophorectomy with or without hysterectomy) or tubal ligation at least six weeks before taking study treatment | 1 | [
"Female",
"sterilization",
"(",
"have",
"had",
"surgical",
"bilateral",
"oophorectomy",
"with",
"or",
"without",
"hysterectomy",
")",
"or",
"tubal",
"ligation",
"at",
"least",
"six",
"weeks",
"before",
"taking",
"study",
"treatment"
] | [
0,
0,
0,
0,
0,
1,
1,
1,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT03070184 | 1:14:chronic_disease,, | Renal disease (eGFR < 60ml/min/1.73m2) | 1 | [
"Renal",
"disease",
"(",
"eGFR",
"<",
"60ml/min/1.73m2",
")"
] | [
2,
2,
0,
0,
0,
0,
0
] |
NCT02393794 | 44:81:treatment,83:97:treatment,99:114:treatment,116:131:treatment,133:149:treatment | Subject has previously been treated with a Histone deacetylases (HDAC) inhibitor, PD-1 inhibitor, PD-L1 inhibitor, PD-L2 inhibitor, CTLA-4 inhibitor | 1 | [
"Subject",
"has",
"previously",
"been",
"treated",
"with",
"a",
"Histone",
"deacetylases",
"(",
"HDAC",
")",
"inhibitor",
",",
"PD-1",
"inhibitor",
",",
"PD-L1",
"inhibitor",
",",
"PD-L2",
"inhibitor",
",",
"CTLA-4",
"inhibitor"
] | [
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
1,
0,
0,
0,
1,
1,
0,
1,
1,
0,
1,
1,
0,
1,
1
] |
NCT02806570 | 54:93:treatment,97:145:treatment,150:188:treatment | Implant or revision of any rhythm management device (cardiac resynchronization therapy (CRT) or cardiac resynchronization therapy device (CRT-D)) or implantable cardioverter defibrillator within the prior month | 1 | [
"Implant",
"or",
"revision",
"of",
"any",
"rhythm",
"management",
"device",
"(",
"cardiac",
"resynchronization",
"therapy",
"(",
"CRT",
")",
"or",
"cardiac",
"resynchronization",
"therapy",
"device",
"(",
"CRT-D",
")",
")",
"or",
"implantable",
"cardioverter",
"defibrillator",
"within",
"the",
"prior",
"month"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
0,
0,
0,
0
] |
NCT02585973 | 4:13:treatment | Co-treatment with weak inhibitors of CYP3A4 | 1 | [
"Co-treatment",
"with",
"weak",
"inhibitors",
"of",
"CYP3A4"
] | [
1,
0,
0,
0,
0,
0
] |
NCT02008656 | 4:34:treatment | No prior pelvic radiation therapy | 1 | [
"No",
"prior",
"pelvic",
"radiation",
"therapy"
] | [
0,
1,
1,
1,
1
] |
NCT02159703 | 7:19:treatment, | Prior chemotherapy within the past 5 years | 1 | [
"Prior",
"chemotherapy",
"within",
"the",
"past",
"5",
"years"
] | [
0,
1,
0,
0,
0,
0,
0
] |
NCT02502253 | 87:97:treatment | Deemed too unstable medically or neurologically to safely enroll in trial of research medication | 1 | [
"Deemed",
"too",
"unstable",
"medically",
"or",
"neurologically",
"to",
"safely",
"enroll",
"in",
"trial",
"of",
"research",
"medication"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02366481 | 37:51:treatment, | Subjects who have participated in a clinical study more recently than one month before the current study | 1 | [
"Subjects",
"who",
"have",
"participated",
"in",
"a",
"clinical",
"study",
"more",
"recently",
"than",
"one",
"month",
"before",
"the",
"current",
"study"
] | [
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03149549 | 11:35:chronic_disease | Active or chronic corneal disorder | 1 | [
"Active",
"or",
"chronic",
"corneal",
"disorder"
] | [
0,
0,
2,
2,
2
] |
NCT02576444 | 103:112:treatment | Patient must not have a co-morbid condition(s) that, in the opinion of the investigator, prevent safe treatment | 1 | [
"Patient",
"must",
"not",
"have",
"a",
"co-morbid",
"condition",
"(",
"s",
")",
"that",
",",
"in",
"the",
"opinion",
"of",
"the",
"investigator",
",",
"prevent",
"safe",
"treatment"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02214667 | 1:20:chronic_disease | delusional disorder | 1 | [
"delusional",
"disorder"
] | [
2,
2
] |
NCT02895945 | 8:44:chronic_disease,, | Severe chronic liver dysfunction or disease (e.g., ≥ 5 × upper limit of normal [ULN] alanine aminotransferase [ALT], as confirmed by central laboratory at screening | 1 | [
"Severe",
"chronic",
"liver",
"dysfunction",
"or",
"disease",
"(",
"e.g.",
",",
"≥",
"5",
"×",
"upper",
"limit",
"of",
"normal",
"[",
"ULN",
"]",
"alanine",
"aminotransferase",
"[",
"ALT",
"]",
",",
"as",
"confirmed",
"by",
"central",
"laboratory",
"at",
"screening"
] | [
0,
2,
2,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03016130 | 30:34:treatment | Underlying diagnosis for non-HSCT patients | 1 | [
"Underlying",
"diagnosis",
"for",
"non-HSCT",
"patients"
] | [
0,
0,
0,
1,
0
] |
NCT02512926 | 1:25:treatment | Myelosuppressive therapy | 1 | [
"Myelosuppressive",
"therapy"
] | [
1,
1
] |
NCT01570998 | 1:25:treatment | prior in-field radiation | 1 | [
"prior",
"in-field",
"radiation"
] | [
1,
1,
1
] |
NCT00875342 | 8:26:treatment,39:64:treatment,66:81:treatment,86:112:treatment | Taking oral anticoagulant medication, ethionamide (Trecator-SC), isoniazid (INH), or anti-depressant medication | 1 | [
"Taking",
"oral",
"anticoagulant",
"medication",
",",
"ethionamide",
"(",
"Trecator-SC",
")",
",",
"isoniazid",
"(",
"INH",
")",
",",
"or",
"anti-depressant",
"medication"
] | [
0,
1,
1,
0,
0,
1,
1,
0,
0,
0,
1,
1,
0,
0,
0,
0,
1,
1
] |
NCT02945800 | 36:48:cancer,50:63:cancer,68:84:cancer,92:128:cancer | have had a histologic diagnosis of osteosarcoma, Ewing sarcoma, or rhabdomyosarcoma or non-rhabdomyosarcoma soft tissue sarcoma either at diagnosis or relapse | 1 | [
"have",
"had",
"a",
"histologic",
"diagnosis",
"of",
"osteosarcoma",
",",
"Ewing",
"sarcoma",
",",
"or",
"rhabdomyosarcoma",
"or",
"non-rhabdomyosarcoma",
"soft",
"tissue",
"sarcoma",
"either",
"at",
"diagnosis",
"or",
"relapse"
] | [
0,
0,
0,
0,
0,
0,
3,
0,
3,
3,
0,
0,
3,
3,
3,
3,
0,
0,
0,
0,
0,
0,
0
] |
NCT02535923 | 61:70:treatment | Sufficient clinical stability to participate as deemed by a treatment provider | 1 | [
"Sufficient",
"clinical",
"stability",
"to",
"participate",
"as",
"deemed",
"by",
"a",
"treatment",
"provider"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0
] |
NCT02111850 | 58:94:allergy_name | History of severe immediate hypersensitivity reaction to any of the agents used in this study | 1 | [
"History",
"of",
"severe",
"immediate",
"hypersensitivity",
"reaction",
"to",
"any",
"of",
"the",
"agents",
"used",
"in",
"this",
"study"
] | [
0,
0,
0,
0,
0,
0,
0,
4,
4,
4,
4,
4,
4,
4,
4
] |
NCT02048371 | 52:63:cancer | Patients with documentation of well differentiated liposarcoma only (of the well differentiated/dedifferentiated liposarcoma family) are specifically excluded, owing to its characteristically slow growth | 1 | [
"Patients",
"with",
"documentation",
"of",
"well",
"differentiated",
"liposarcoma",
"only",
"(",
"of",
"the",
"well",
"differentiated/dedifferentiated",
"liposarcoma",
"family",
")",
"are",
"specifically",
"excluded",
",",
"owing",
"to",
"its",
"characteristically",
"slow",
"growth"
] | [
0,
0,
0,
0,
0,
0,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01389024 | 19:43:chronic_disease | Other significant organ system dysfunction | 1 | [
"Other",
"significant",
"organ",
"system",
"dysfunction"
] | [
0,
0,
2,
2,
2
] |
NCT02724540 | 22:49:treatment | Contraindications to hepatic artery embolization | 1 | [
"Contraindications",
"to",
"hepatic",
"artery",
"embolization"
] | [
0,
0,
1,
1,
1
] |
NCT02122081 | 31:65:chronic_disease | Patients seropositive for the human immunodeficiency virus (HIV) | 1 | [
"Patients",
"seropositive",
"for",
"the",
"human",
"immunodeficiency",
"virus",
"(",
"HIV",
")"
] | [
0,
0,
0,
0,
2,
2,
2,
2,
0,
0
] |
NCT02960555 | 1:21:cancer | Plasma cell leukemia | 1 | [
"Plasma",
"cell",
"leukemia"
] | [
3,
3,
3
] |
NCT01917929 | 15:55:chronic_disease | Patient has a neuromuscular or neurosensory deficiency that would create an unacceptable risk of instability, prosthesis fixation failure or complications in postoperative care, or which limits the ability to evaluate the safety and efficacy of the device | 1 | [
"Patient",
"has",
"a",
"neuromuscular",
"or",
"neurosensory",
"deficiency",
"that",
"would",
"create",
"an",
"unacceptable",
"risk",
"of",
"instability",
",",
"prosthesis",
"fixation",
"failure",
"or",
"complications",
"in",
"postoperative",
"care",
",",
"or",
"which",
"limits",
"the",
"ability",
"to",
"evaluate",
"the",
"safety",
"and",
"efficacy",
"of",
"the",
"device"
] | [
0,
0,
0,
2,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03144206 | 1:17:chronic_disease,83:92:treatment,109:136:chronic_disease,161:181:chronic_disease | Vascular disease resulting in clinically apparent compromise in blood flow to the treatment extremity (i.e. peripheral vascular disease with diminished pulses, venous insufficiency with clinical evidence of vascular congestion) | 1 | [
"Vascular",
"disease",
"resulting",
"in",
"clinically",
"apparent",
"compromise",
"in",
"blood",
"flow",
"to",
"the",
"treatment",
"extremity",
"(",
"i.e",
".",
"peripheral",
"vascular",
"disease",
"with",
"diminished",
"pulses",
",",
"venous",
"insufficiency",
"with",
"clinical",
"evidence",
"of",
"vascular",
"congestion",
")"
] | [
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
2,
2,
2,
0,
0,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0
] |
NCT02451982 | 1:22:chronic_disease | Stage I or II disease | 1 | [
"Stage",
"I",
"or",
"II",
"disease"
] | [
2,
2,
2,
2,
2
] |
NCT02670837 | 5:31:treatment | Off immune suppressive therapy | 1 | [
"Off",
"immune",
"suppressive",
"therapy"
] | [
0,
1,
1,
1
] |
NCT02004275 | 65:74:treatment | Previous hypersensitivity to any of the components of the study treatment | 1 | [
"Previous",
"hypersensitivity",
"to",
"any",
"of",
"the",
"components",
"of",
"the",
"study",
"treatment"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT01648023 | 28:50:treatment,63:73:treatment,75:86:treatment,91:100:treatment | Patients who have received prior systemic therapy with either irinotecan, gemcitabine, or cisplatin | 1 | [
"Patients",
"who",
"have",
"received",
"prior",
"systemic",
"therapy",
"with",
"either",
"irinotecan",
",",
"gemcitabine",
",",
"or",
"cisplatin"
] | [
0,
0,
0,
0,
1,
1,
1,
0,
0,
1,
0,
1,
0,
0,
1
] |
NCT02264678 | 17:24:allergy_name | Bad reaction to AZD6738 | 1 | [
"Bad",
"reaction",
"to",
"AZD6738"
] | [
0,
0,
0,
4
] |
NCT02101736 | 21:33:treatment, | No myelosuppressive chemotherapy within 4 weeks of study entry | 1 | [
"No",
"myelosuppressive",
"chemotherapy",
"within",
"4",
"weeks",
"of",
"study",
"entry"
] | [
0,
0,
1,
0,
0,
0,
0,
0,
0
] |
NCT01925131 | 1:22:treatment, | Monoclonal antibodies must not have been received for 1 week prior to registration | 1 | [
"Monoclonal",
"antibodies",
"must",
"not",
"have",
"been",
"received",
"for",
"1",
"week",
"prior",
"to",
"registration"
] | [
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02582827 | ,,,,,241:267:treatment, | QTc prolongation defined as a QTc interval according to Bazett's formula of ≥ 450 msec for male patients or ≥470 msec for female patients at Baseline. Interval determination will be based on a mean value obtained from 3 sequential baseline electrocardiographs (ECGs) obtained at least 5 minutes apart | 1 | [
"QTc",
"prolongation",
"defined",
"as",
"a",
"QTc",
"interval",
"according",
"to",
"Bazett",
"'s",
"formula",
"of",
"≥",
"450",
"msec",
"for",
"male",
"patients",
"or",
"≥470",
"msec",
"for",
"female",
"patients",
"at",
"Baseline",
".",
"Interval",
"determination",
"will",
"be",
"based",
"on",
"a",
"mean",
"value",
"obtained",
"from",
"3",
"sequential",
"baseline",
"electrocardiographs",
"(",
"ECGs",
")",
"obtained",
"at",
"least",
"5",
"minutes",
"apart"
] | [
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0
] |