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NCT02593123 | 23:26:chronic_disease | Negative serology for HIV | 1 | [
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NCT02578641 | 1:4:chronic_disease | HIV Positive | 1 | [
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NCT02578641 | 11:14:chronic_disease, | Status of HIV must be confirmed via a HIV antibody test or other confirmatory tests available within 12 months before screening or at screening | 1 | [
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NCT02567422 | 33:36:chronic_disease | patients with poorly controlled HIV | 1 | [
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NCT02566395 | 1:4:chronic_disease | HIV positive | 1 | [
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NCT02566304 | 1:4:chronic_disease | HIV positive | 1 | [
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NCT02552953 | 13:16:chronic_disease | Known to be HIV-positive | 1 | [
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NCT02543983 | 10:13:chronic_disease | Positive HIV test | 1 | [
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NCT02542202 | 1:4:chronic_disease | HIV testing is not required for eligibility for this protocol | 1 | [
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NCT02541903 | 7:10:chronic_disease | known HIV carrier | 1 | [
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NCT02531932 | 20:23:chronic_disease | A known history of HIV seropositivity | 1 | [
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NCT02531880 | 19:22:chronic_disease | Positive test for HIV | 1 | [
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NCT02531295 | ,,37:40:chronic_disease | Pre-ART viral load <2000 copies/ml (HIV controllers) | 1 | [
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NCT02529644 | ,143:146:chronic_disease | Minors 18 and under are intentionally excluded since the intervention study has been designed specifically for adults with information of how HIV affects the African American adult population | 1 | [
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NCT02520427 | 24:27:chronic_disease | Known positiv test for HIV | 1 | [
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NCT02515708 | 1:4:chronic_disease | HIV positive patient | 1 | [
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NCT02508038 | 1:4:chronic_disease | HIV infection | 1 | [
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NCT02472834 | 1:4:chronic_disease | HIV positive | 1 | [
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NCT02457845 | 7:10:chronic_disease | Known HIV seropositivity | 1 | [
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NCT02453113 | 12:15:chronic_disease | History of HIV | 1 | [
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NCT02452268 | 1:4:chronic_disease | HIV positive patients | 1 | [
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NCT02446093 | 13:16:chronic_disease | Known to be HIV+ | 1 | [
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NCT02442297 | 7:10:chronic_disease | Known HIV positivity | 1 | [
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NCT02430077 | 7:10:chronic_disease | Known HIV-infected patient | 1 | [
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NCT02408861 | 1:4:chronic_disease,, | HIV viral load should be well suppressed, defined as below the limit of detection of the local assay or below 75 copies/mL by Food and Drug Administration (FDA)-approved assays, within 4 weeks prior to registration | 1 | [
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NCT02400463 | 7:10:chronic_disease | known HIV infection | 1 | [
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NCT02393690 | 22:25:chronic_disease | patients known to be HIV positive, but without clinical evidence of an immunocompromised state, are eligible for this trial | 1 | [
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NCT02384954 | 5:8:chronic_disease | Not HIV positive | 1 | [
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NCT02379520 | 7:10:chronic_disease | Known HIV positivity | 1 | [
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NCT02374333 | 1:4:chronic_disease | HIV infection | 1 | [
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NCT02374021 | 1:4:chronic_disease | HIV | 1 | [
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NCT02369406 | ,,39:42:chronic_disease,,, | 57-365 days after birth if infant was HIV-negative based on testing performed within 96 hours after birth (or if unknown HIV status < 96 hours from birth) and then found to be HIV-positive based on testing performed between 96 hours and 42 days after birth | 1 | [
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NCT02369406 | 1:4:chronic_disease, | HIV-infection identified by testing conducted within 96 hours after birth | 1 | [
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NCT02369406 | 1:4:chronic_disease, | HIV-negative within 96 hours after birth | 1 | [
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NCT02369406 | 1:4:chronic_disease,, | HIV-positive between 96 hours and 42 days after birth | 1 | [
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NCT02362997 | 1:4:chronic_disease | HIV-positive | 1 | [
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NCT02358187 | 1:4:chronic_disease | HIV-positive patients | 1 | [
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NCT02350764 | 23:26:chronic_disease | Any positive test for HIV | 1 | [
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NCT02347891 | 30:33:chronic_disease | Have a historically positive HIV test or test positive at screening for HIV | 1 | [
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NCT02344355 | 7:10:chronic_disease | Known HIV-positive individuals | 1 | [
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NCT02340156 | 23:26:chronic_disease | Positive results from HIV serology testing, if any available | 1 | [
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NCT02335138 | 48:51:chronic_disease | Either partner expresses unwillingness to have HIV test kits delivered to a home address | 1 | [
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NCT02335138 | 52:55:chronic_disease | Either partner expresses unwillingness to test for HIV together with his male sexual partner | 1 | [
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NCT02335138 | 21:24:chronic_disease,, | Negative or unknown HIV status and not having tested in the last 6 months, with a partner meeting the same criteria OR in a sero-discordant with the negative/unknown partner reporting not having tested in the past 6 months | 1 | [
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NCT02335138 | 30:33:chronic_disease, | Willingness to be tested for HIV with one's male sexual partner | 1 | [
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NCT02332850 | 7:10:chronic_disease | Known HIV seropositivity | 1 | [
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NCT02329652 | 1:4:chronic_disease | HIV | 1 | [
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NCT02321501 | 18:21:chronic_disease | Known history of HIV seropositivity | 1 | [
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NCT02312596 | 1:4:chronic_disease | HIV | 1 | [
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NCT02296684 | 18:21:chronic_disease | Known history of HIV (HIV 1/2 antibodies) | 1 | [
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NCT02256631 | 22:25:chronic_disease, | At increased risk of HIV acquisition defined as documentation of one or more of the following risk factors | 1 | [
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NCT02256631 | 47:50:chronic_disease,, | Mother with any detectable viral replication (HIV RNA above the limit of detection) at last measurement prior to delivery determined within 30 days of delivery | 1 | [
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NCT02233868 | 17:20:chronic_disease | Have a positive HIV test (clinical laboratory results, medical history) | 1 | [
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NCT02203903 | 15:18:chronic_disease | Patients with HIV infection | 1 | [
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NCT02203513 | 1:4:chronic_disease,,, | HIV- positive patients who are not on HAART and have CD4 counts > 500 will be considered on an individual basis | 1 | [
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NCT02186418 | 21:24:chronic_disease | Sero-positivity for HIV | 1 | [
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NCT02179359 | 1:4:chronic_disease | HIV positive | 1 | [
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NCT02164422 | 45:48:chronic_disease | other unstable medical conditions including HIV | 1 | [
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NCT02159027 | ,,125:128:chronic_disease | score of < -0.5 OR a neurocognitive abnormality (< -0.5) in at least one cognitive domain known to be typically affected by HIV | 1 | [
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NCT02140255 | 11:14:chronic_disease | Confirmed HIV infection defined as positive results from two samples collected at different time points | 1 | [
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NCT02140255 | 21:24:chronic_disease, | No confirmed plasma HIV RNA greater than or equal to 200 copies/mL at Step 2 Week 24 and up to but excluding Step 2 Week 48 (see the study protocol for procedural guidance related to this criterion) | 1 | [
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NCT02140255 | 11:14:chronic_disease, | No plasma HIV RNA detected by testing performed at the local CLIA-certified (US sites) or VQA-certified (non-US sites) laboratory, after criteria above have been confirmed, with specimen collection for the assay within 14 days prior to Step 3 Entry | 1 | [
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NCT02140255 | 8:11:chronic_disease | Plasma HIV RNA greater than or equal to LOD based on standard quantitative testing performed at the local CLIA-certified (US sites) or VQA-certified (non-US sites) laboratory after ART cessation (see the study protocol for procedural guidance related to this criterion) | 1 | [
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NCT02140255 | 10:13:chronic_disease | Presumed HIV infection defined as greater than or equal to one positive rapid HIV antibody test obtained in the peripartum period | 1 | [
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NCT02140255 | 17:20:chronic_disease,, | Two consecutive HIV DNA tests with no DNA detected in at least 850,000 PBMCs assayed (performed in the study's designated central laboratory) at least 8 weeks apart | 1 | [
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NCT02140255 | 26:29:chronic_disease, | Two consecutive negative HIV antibody tests by fourth generation enzyme-linked immunosorbent assay (ELISA) (performed in the study's designated central laboratory) at least 8 weeks apart | 1 | [
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NCT02133196 | 18:21:chronic_disease | Seronegative for HIV antibody | 1 | [
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NCT02128906 | 1:4:chronic_disease | HIV testing is not required for entry into this protocol | 1 | [
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NCT02128100 | 1:4:chronic_disease | HIV testing is not manditory for this protocol | 1 | [
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NCT02124902 | 7:10:chronic_disease | Known HIV-positivity | 1 | [
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NCT02106988 | 13:16:chronic_disease | known to be HIV positive | 1 | [
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NCT02105766 | 1:4:chronic_disease | HIV positive | 1 | [
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NCT02101736 | 1:4:chronic_disease | HIV testing will not be required as part of this trial, unless HIV is clinically suspected | 1 | [
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NCT02100891 | 1:4:chronic_disease | HIV seropositive patients | 1 | [
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NCT02100891 | 1:4:chronic_disease | HIV-positive donors | 1 | [
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NCT02081404 | 15:18:chronic_disease | Patients with HIV | 1 | [
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NCT02078102 | 31:34:chronic_disease | Patients must be negative for HIV | 1 | [
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NCT02075710 | 10:13:chronic_disease | positive HIV antibody test or hepatitis serologies | 1 | [
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NCT02059239 | 26:29:chronic_disease | Known to be positive for HIV | 1 | [
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NCT01976169 | 10:13:chronic_disease | Baseline HIV screening | 1 | [
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NCT01962415 | 1:4:chronic_disease | HIV negative | 1 | [
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NCT01956084 | 7:10:chronic_disease | Donor HIV negative | 1 | [
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NCT01956084 | 16:19:chronic_disease | Donors who are HIV positive | 1 | [
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NCT01953900 | 1:4:chronic_disease | HIV positivity | 1 | [
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NCT01928576 | 1:4:chronic_disease | HIV-positive patients are excluded | 1 | [
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NCT01925378 | 31:34:chronic_disease, | Patients must have a negative HIV test within 14 days of starting the NFV | 1 | [
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NCT01920737 | 7:10:chronic_disease | Known HIV positive status | 1 | [
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NCT01913106 | 1:4:chronic_disease | HIV + patients | 1 | [
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NCT01896999 | 1:4:chronic_disease | HIV viral loads undetectable by standard clinical HIV testing | 1 | [
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NCT01760655 | 1:4:chronic_disease | HIV positive | 1 | [
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NCT01734512 | 20:23:chronic_disease | A known history of HIV seropositivity | 1 | [
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NCT01730937 | 1:4:chronic_disease,, | HIV positive with CD4 count < (350) cells/microliter | 1 | [
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