Dataset Viewer
ID
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11
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777
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1.5k
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int64 1
3
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sequence | ner_tags
sequence |
---|---|---|---|---|---|
NCT02105766
|
8:16:chronic_disease,20:32:treatment
|
portal fibrosis by liver biopsy
| 1 |
[
"portal",
"fibrosis",
"by",
"liver",
"biopsy"
] |
[
0,
2,
0,
1,
1
] |
NCT03008070
|
22:34:treatment
|
Contra-indication to liver biopsy
| 1 |
[
"Contra-indication",
"to",
"liver",
"biopsy"
] |
[
0,
0,
1,
1
] |
NCT03008070
|
,32:44:treatment,,
|
Have a stable weight since the liver biopsy was performed defined by no more than a 5 % loss of initial body weight
| 1 |
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"Have",
"a",
"stable",
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0,
0
] |
NCT03008070
|
26:38:treatment,
|
Subject agrees to have a liver biopsy performed after 24 weeks of treatment
| 1 |
[
"Subject",
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"a",
"liver",
"biopsy",
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0,
0,
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NCT02515708
|
,43:55:treatment,
|
Liver steatosis (on visual estimate or on liver biopsy) > 30%
| 1 |
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0
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NCT02474199
|
85:97:treatment,,
|
For subjects with elevated liver tests as defined above, local pathology reading of liver biopsy 6-10 days after darTregs infusion is without AR according to Banff criteria
| 1 |
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NCT02474199
|
11:23:treatment
|
Screening liver biopsy with any of the following histological criteria, as determined by the reading of a central pathologist
| 1 |
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NCT02412540
|
,,42:54:treatment,
|
Weight reduction of >5% between baseline liver biopsy and enrollment, as weight loss >5% may change NASH severity
| 1 |
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NCT02094794
|
1:22:treatment,26:61:treatment,,
|
Echocardiogram (ECHO) or multi gated acquisition scan (MUGA): ejection fraction of >= 50%
| 1 |
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"Echocardiogram",
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] |
NCT02257138
|
85:98:treatment,116:138:treatment
|
patients with newly diagnosed or previously treated disease are eligible as long as prior therapy does not include hypomethylating agents
| 1 |
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NCT03126110
|
,54:67:treatment
|
Has not recovered to ≤ Grade 1 from toxic effects of prior therapy
| 1 |
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NCT03104699
|
32:45:treatment,,
|
Persisting toxicity related to prior therapy of NCI CTCAE grade >1 severity
| 1 |
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NCT03007030
|
13:26:treatment
|
Any line of prior therapy
| 1 |
[
"Any",
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"therapy"
] |
[
0,
0,
0,
1,
1
] |
NCT02942095
|
28:41:treatment,,
|
Patient who were receiving prior therapy will require wash out period of either more than 2 weeks or more than 5 half-lives whichever shorter
| 1 |
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0
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NCT02932280
|
52:65:treatment,
|
have recovered from the acute toxic effects of all prior therapy to ≤ grade 1 before entering this study
| 1 |
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NCT02912572
|
,,42:55:treatment
|
Persisting Grade >=2 toxicity related to prior therapy
| 1 |
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"=2",
"toxicity",
"related",
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0,
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0,
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1,
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NCT02584647
|
11:24:treatment
|
Allowable prior therapy
| 1 |
[
"Allowable",
"prior",
"therapy"
] |
[
0,
1,
1
] |
NCT02553460
|
9:22:treatment
|
Limited prior therapy
| 1 |
[
"Limited",
"prior",
"therapy"
] |
[
0,
1,
1
] |
NCT02425904
|
49:62:treatment
|
There is no limitation of amount or the type of prior therapy or drugs
| 1 |
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NCT02392572
|
51:64:treatment,
|
Persistent clinically significant toxicities from prior therapy must not be greater than grade 1
| 1 |
[
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NCT02383927
|
34:47:treatment
|
has relapsed or is refractory to prior therapy
| 1 |
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] |
NCT02370693
|
,,,,58:71:treatment
|
Fall in FVC > 10% over 6 months on at least 12 months of prior therapy
| 1 |
[
"Fall",
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"10",
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NCT02340156
|
61:74:treatment
|
Radiographic demonstration of disease progression following prior therapy
| 1 |
[
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"progression",
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0,
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1,
1
] |
NCT02315612
|
67:80:treatment
|
Subjects must have recovered from the acute side effects of their prior therapy, such that eligibility criteria are met
| 1 |
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NCT02302235
|
,,62:75:treatment
|
Failure to recover from <CTCAE grade 2 toxicities related to prior therapy
| 1 |
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NCT02192359
|
42:55:treatment
|
Any clinically significant toxicity from prior therapy must have improved to grade 0 or grade 1
| 1 |
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NCT02159495
|
39:52:treatment,
|
Non hematological toxicity related to prior therapy must either have returned to =< grade 2, baseline, or deemed irreversible
| 1 |
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NCT02146924
|
39:52:treatment,
|
Non-hematological toxicity related to prior therapy must either have returned to =< grade 3, baseline, or deemed irreversible
| 1 |
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NCT02101034
|
,49:62:treatment
|
Minimum of 14 days elapsed since the end of any prior therapy
| 1 |
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NCT02013336
|
27:40:treatment
|
Disease progression after prior therapy in locally advanced or metastatic setting
| 1 |
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NCT01954576
|
36:49:treatment,,
|
Recovery from the toxic effects of prior therapy to not more than grade 1 or >3 weeks from prior therapy to registration, whichever is later
| 1 |
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NCT01906385
|
30:43:treatment,,
|
Recovered from toxicities of prior therapy to grade 0 or 1
| 1 |
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NCT01896999
|
5:18:treatment,
|
All prior therapy must have been completed at least 21 days prior to enrollment
| 1 |
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NCT01865162
|
,,62:75:treatment
|
Failure to recover from <CTCAE grade 2 toxicities related to prior therapy
| 1 |
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NCT01849146
|
35:48:treatment
|
recovered from severe toxicity of prior therapy
| 1 |
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NCT01553071
|
49:62:treatment
|
Patients must have recovered from toxicities of prior therapy
| 1 |
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0,
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NCT01430390
|
67:80:treatment
|
Subjects must have recovered from the acute side effects of their prior therapy, such that eligibility criteria are met
| 1 |
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NCT01371630
|
9:22:treatment
|
minimal prior therapy
| 1 |
[
"minimal",
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] |
[
0,
1,
1
] |
NCT01037790
|
74:87:treatment,
|
The subject has not recovered from clinically-meaningful toxicity due to prior therapy (i.e., back to baseline or Grade ≤ 1)
| 1 |
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NCT00412594
|
79:92:treatment
|
Patients with relapsed disease are eligible if they have had no more than one prior therapy
| 1 |
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NCT00004317
|
,25:38:treatment
|
No more than 1 month of prior therapy
| 1 |
[
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] |
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0,
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] |
NCT02542202
|
18:21:chronic_disease,69:128:treatment,,,
|
patients who are HIV positive are eligible, provided they are under treatment with highly active antiretroviral therapy (HAART) and have a CD4 count >= 200 cells/microliter within 30 days prior to registration
| 1 |
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NCT02346253
|
1:4:chronic_disease,61:120:treatment,,,
|
HIV-positive patients are eligible, provided they are under treatment with highly active antiretroviral therapy (HAART) and have a CD4 count >= 200 cells/microliter no more than 30 days prior to registration
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NCT03175159
|
1:4:chronic_disease
|
HIV-uninfected
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[
"HIV-uninfected"
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[
2
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NCT03175159
|
26:29:chronic_disease
|
Involvement in any other HIV Prevention study that may interfere with the ability to test major study outcomes
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NCT03167606
|
1:4:chronic_disease
|
HIV+
| 1 |
[
"HIV+"
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[
2
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NCT03167606
|
13:16:chronic_disease
|
Self-report HIV-negative or unknown status
| 1 |
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[
0,
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0,
0,
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NCT03157167
|
16:19:chronic_disease
|
The subject is HIV positive
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NCT03135886
|
17:20:chronic_disease
|
are offered any HIV and/or HCV tests
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NCT03132415
|
1:4:chronic_disease
|
HIV-positive
| 1 |
[
"HIV-positive"
] |
[
2
] |
NCT03132415
|
16:19:chronic_disease
|
Self-report as HIV-negative or sero-status unaware
| 1 |
[
"Self-report",
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"unaware"
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[
0,
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2,
0,
0,
0
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NCT03109431
|
23:26:chronic_disease
|
Acutely infected with HIV
| 1 |
[
"Acutely",
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"HIV"
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[
0,
0,
0,
2
] |
NCT03109431
|
1:4:chronic_disease
|
HIV-negative (high-risk HIV-negative youth will be invited to participate in another study)
| 1 |
[
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NCT03109431
|
1:4:chronic_disease
|
HIV-positive serostatus
| 1 |
[
"HIV-positive",
"serostatus"
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[
2,
0
] |
NCT03088709
|
14:17:chronic_disease
|
Positive for HIV
| 1 |
[
"Positive",
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"HIV"
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[
0,
0,
2
] |
NCT03086057
|
1:4:chronic_disease
|
HIV Positive at baseline
| 1 |
[
"HIV",
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"baseline"
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[
2,
0,
0,
0
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NCT03081559
|
38:41:chronic_disease
|
Evidence of suboptimal engagement in HIV care, as indicated by one or more
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[
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2,
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0,
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NCT03081559
|
1:4:chronic_disease
|
HIV+ confirmed via antibody testing
| 1 |
[
"HIV+",
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[
2,
0,
0,
0,
0
] |
NCT03081559
|
14:17:chronic_disease,
|
Reporting no HIV primary care appointments in the prior 6 months
| 1 |
[
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NCT03078153
|
1:4:chronic_disease
|
HIV negative
| 1 |
[
"HIV",
"negative"
] |
[
2,
0
] |
NCT03078153
|
1:4:chronic_disease
|
HIV positive
| 1 |
[
"HIV",
"positive"
] |
[
2,
0
] |
NCT03078153
|
27:30:chronic_disease
|
Not enrolled in any other HIV prevention trial
| 1 |
[
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[
0,
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0,
2,
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0
] |
NCT03060772
|
1:4:chronic_disease
|
HIV-positive
| 1 |
[
"HIV-positive"
] |
[
2
] |
NCT03059355
|
23:26:chronic_disease
|
Be serum positive for HIV
| 1 |
[
"Be",
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[
0,
0,
0,
0,
2
] |
NCT03056339
|
29:32:chronic_disease
|
Known positive serology for HIV
| 1 |
[
"Known",
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"for",
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[
0,
0,
0,
0,
2
] |
NCT03004170
|
96:99:chronic_disease,
|
Report engaging in one or more occasions of condomless anal and/or vaginal intercourse with an HIV-negative or unknown HIV serostatus sex partner in the 3 months prior to study enrollment
| 1 |
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NCT02979366
|
12:15:chronic_disease
|
arriers of HIV antibodies
| 1 |
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[
0,
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NCT02953509
|
1:4:chronic_disease
|
HIV
| 1 |
[
"HIV"
] |
[
2
] |
NCT02944578
|
1:4:chronic_disease,
|
HIV negative women
| 1 |
[
"HIV",
"negative",
"women"
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[
2,
0,
0
] |
NCT02944578
|
1:4:chronic_disease,
|
HIV positive women
| 1 |
[
"HIV",
"positive",
"women"
] |
[
2,
0,
0
] |
NCT02929069
|
1:4:chronic_disease,,
|
HIV sexual risk (≥1 act of condomless anal with a male partner of unknown status or HIV+ status, unless with HIV+ partner with known undetectable viral load)
| 1 |
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NCT02929069
|
1:4:chronic_disease
|
HIV-negative status
| 1 |
[
"HIV-negative",
"status"
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[
2,
0
] |
NCT02929069
|
1:4:chronic_disease
|
HIV-positive status
| 1 |
[
"HIV-positive",
"status"
] |
[
2,
0
] |
NCT02915744
|
1:4:chronic_disease
|
HIV
| 1 |
[
"HIV"
] |
[
2
] |
NCT02907944
|
27:30:chronic_disease,
|
Employed at participating HIV clinic for at least 6 months
| 1 |
[
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0,
0,
0,
0
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NCT02907944
|
1:4:chronic_disease
|
HIV-infected
| 1 |
[
"HIV-infected"
] |
[
2
] |
NCT02907944
|
11:14:chronic_disease
|
Receiving HIV care in the index clinic
| 1 |
[
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[
0,
2,
0,
0,
0,
0,
0
] |
NCT02895945
|
1:4:chronic_disease,,
|
HIV+ with stable disease and CD4+ count ≥ 200 cells/mm^3 at screening
| 1 |
[
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0
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NCT02848417
|
1:4:chronic_disease
|
HIV
| 1 |
[
"HIV"
] |
[
2
] |
NCT02835729
|
7:10:chronic_disease
|
Known HIV-infected patients
| 1 |
[
"Known",
"HIV-infected",
"patients"
] |
[
0,
2,
0
] |
NCT02833805
|
1:4:chronic_disease
|
HIV seropositivity
| 1 |
[
"HIV",
"seropositivity"
] |
[
2,
0
] |
NCT02820350
|
1:4:chronic_disease
|
HIV
| 1 |
[
"HIV"
] |
[
2
] |
NCT02801747
|
27:30:chronic_disease,,,
|
Sub-optimal engagement in HIV care (assessed from the medical record, defined as less than 1 visit in every 4-mo. period in the past year [two of them at least 90 days apart], pro-rated for those diagnosed less than a year ago) or > 2 missed visits (without prior cancellation) in the past year
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NCT02797262
|
1:4:chronic_disease
|
HIV-infected individuals in HIV care
| 1 |
[
"HIV-infected",
"individuals",
"in",
"HIV",
"care"
] |
[
2,
0,
0,
0,
0
] |
NCT02796027
|
23:26:chronic_disease
|
positive confirmatory HIV test
| 1 |
[
"positive",
"confirmatory",
"HIV",
"test"
] |
[
0,
0,
2,
0
] |
NCT02772562
|
51:54:chronic_disease
|
immunocompromised individuals, such as those with HIV
| 1 |
[
"immunocompromised",
"individuals",
",",
"such",
"as",
"those",
"with",
"HIV"
] |
[
0,
0,
0,
0,
0,
0,
0,
2
] |
NCT02770547
|
1:4:chronic_disease
|
HIV positive
| 1 |
[
"HIV",
"positive"
] |
[
2,
0
] |
NCT02770326
|
1:4:chronic_disease,,
|
HIV infection with CD4 count <240
| 1 |
[
"HIV",
"infection",
"with",
"CD4",
"count",
"<",
"240"
] |
[
2,
0,
0,
0,
0,
0,
0
] |
NCT02766998
|
1:4:chronic_disease
|
HIV positive mothers
| 1 |
[
"HIV",
"positive",
"mothers"
] |
[
2,
0,
0
] |
NCT02764853
|
1:4:chronic_disease
|
HIV-positive
| 1 |
[
"HIV-positive"
] |
[
2
] |
NCT02759575
|
1:4:chronic_disease
|
HIV
| 1 |
[
"HIV"
] |
[
2
] |
NCT02734771
|
24:27:chronic_disease
|
Patient is known to be HIV positive (test result not required for enrollment)
| 1 |
[
"Patient",
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"to",
"be",
"HIV",
"positive",
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"test",
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[
0,
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0,
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02660528
|
1:4:chronic_disease
|
HIV
| 1 |
[
"HIV"
] |
[
2
] |
NCT02641093
|
1:4:chronic_disease
|
HIV
| 1 |
[
"HIV"
] |
[
2
] |
NCT02635360
|
18:21:chronic_disease
|
Known history of HIV
| 1 |
[
"Known",
"history",
"of",
"HIV"
] |
[
0,
0,
0,
2
] |
NCT02629120
|
1:4:chronic_disease
|
HIV positive
| 1 |
[
"HIV",
"positive"
] |
[
2,
0
] |
NCT02629120
|
9:12:chronic_disease
|
Must be HIV negative
| 1 |
[
"Must",
"be",
"HIV",
"negative"
] |
[
0,
0,
2,
0
] |
NCT02610374
|
1:4:chronic_disease
|
HIV-infected cohort (Cohort A)
| 1 |
[
"HIV-infected",
"cohort",
"(",
"Cohort",
"A",
")"
] |
[
2,
0,
0,
0,
0,
0
] |
NCT02610374
|
1:4:chronic_disease
|
HIV-negative cohorts (Cohort B and C)
| 1 |
[
"HIV-negative",
"cohorts",
"(",
"Cohort",
"B",
"and",
"C",
")"
] |
[
2,
0,
0,
0,
0,
0,
0,
0
] |
NCT02600273
|
10:13:chronic_disease
|
Unstable HIV or associated comorbidities, as determined by a licensed medical professional
| 1 |
[
"Unstable",
"HIV",
"or",
"associated",
"comorbidities",
",",
"as",
"determined",
"by",
"a",
"licensed",
"medical",
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] |
[
0,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
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