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COMPLETED

Sustainable Healthcenter Implementation PrEP Pilot Study

NCT02074891 · View on ClinicalTrials.gov ↗

Study Summary

A health services implementation pilot study, conducted with an observational cohort of HIV-uninfected persons including men who have sex with men, heterosexual women and men, and injection drug users receiving daily oral antiretroviral preexposure prophylaxis (PrEP) at four federally qualified health centers that provide sexual health and primary care services to communities with high HIV incidence/prevalence.

Interventions

  • DRUG coformulated TDF/FTC

Study Locations (5)

Illinois

  • Access Community Health Network - Grand Boulevard Health and Specialty Center — Chicago
  • Howard Brown Community Health Center — Chicago

District of Columbia

  • Whitman Walker Health — Washington D.C.

Mississippi

  • Open Arms Healthcare Center — Jackson

Pennsylvania

  • Strawberry Mansion Health Center — Philadelphia

Trial Details

FieldValue
Enrollment Target 1,420 participants
Start Date 2014-10
Est. Completion 2018-11

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02074891

The ClinicalTrials.gov registry entry for NCT02074891 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,420 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Centers for Disease Control and Prevention, which has 42 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with HIV Chemoprophylaxis appearing as the primary indexed condition, and to 1 intervention — of which coformulated TDF/FTC is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02074891 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Illinois, District of Columbia, Mississippi. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02074891 about?

NCT02074891 is a clinical study titled "Sustainable Healthcenter Implementation PrEP Pilot Study". A health services implementation pilot study, conducted with an observational cohort of HIV-uninfected persons including men who have sex with men, heterosexual women and men, and injection drug users receiving daily oral antiretroviral preexposure prophylaxis (PrEP) at four federally qualified heal...

What is the current status of trial NCT02074891?

This trial is currently completed. The enrollment target is 1,420 participants. The study started on 2014-10. Estimated completion is 2018-11.

What conditions does trial NCT02074891 study?

This clinical trial studies the following conditions: HIV Chemoprophylaxis, HIV Preexposure Prophylaxis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02074891?

The interventions under investigation include: coformulated TDF/FTC (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02074891?

This trial is sponsored by Centers for Disease Control and Prevention, which has 42 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02074891 being conducted?

This trial has 5 study locations across District of Columbia, Illinois, Mississippi, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial