RecruitingNCT01206920
The DC Cohort Longitudinal HIV Status Neutral Study
Development of a City-Wide Cohort of HIV-Infected Persons in Care in the District of Columbia: The DC Cohort
Sponsor
George Washington University
Enrollment
19,000 participants
Start Date
Jan 1, 2011
Study Type
OBSERVATIONAL
Conditions
Summary
The goal of the DC Cohort is to establish a clinic-based city-wide longitudinal cohort that will describe clinical outcomes, and improve the quality of care for patients diagnosed with Human Immunodeficiency Virus/Acquired Immune Deficiency Syndrome (HIV/AIDS) or at higher risk for acquiring HIV and receiving care in Washington, DC.
Eligibility
Inclusion Criteria14
- Patient is receiving care for HIV at one or more of the twelve participating clinics in the DC Cohort.
- Patient is either age 18 years or older, or seeks HIV care independently and is able to understand and sign informed consent.
- Patient is a minor who is consented by a parent or legal guardian.
- Persons receiving any antiretroviral prescription without evidence of HIV or Hepatitis B infection
- PrEP (e.g., TDF/FTC, Descovy, Apretude)
- Combination ART indicative of nPEP in an HIV-uninfected person
- Persons receiving an antiretroviral prescription indicative of DoxyPEP Doxycycline 200mg PO taken within 72 hrs of unprotected sexual encounter (or variations thereof where clearly not prescribed as a treatment course)
- Test positive for ≥1 bacterial STI (positive gonorrhea (GC/NG) or chlamydia (CT) test or positive syphilis test requiring treatment within one year)
- bacterial STI (GC, chlamydia, syphilis) tests at 2 or more different encounters
- HIV tests at 2 or more different encounters
- Patient requesting PrEP at their clinical visit
- Patient requesting nPEP at their clinical visit
- People who identify as injecting drugs
- Patients with a Z29.81 Encounter for HIV pre-exposure prophylaxis
Exclusion Criteria2
- Patient is unable or refuses to provide informed consent.
- Minor children ages 12 through 17 who are unaware of their HIV status
Locations(14)
View Full Details on ClinicalTrials.gov
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NCT01206920
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