Expired Study
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Seattle, Washington 98104


Purpose:

As explained in detail in a recently published hypothesis article (Hladik F. A new hypothesis on HIV cure. F1000Research, 4:77 (2015)), the investigators hypothesize that NRTI drugs may reduce the likelihood of HIV eradication by promoting the survival of cells with integrated provirus. In this study, the investigators will test whether daily oral use of two NTRI drugs, tenofovir and emtricitabine (Truvada Pill), induces changes in the upper and lower gut mucosa that are congruent with supporting this hypothesis.


Criteria:

Inclusion Criteria: - • HIV-negative - Male gender at birth - Age ≥18 years old - Intent to initiate PrEP in the next 1-2 months. - Willingness and ability to provide informed consent for study participation - Willingness to undergo all required study procedures Exclusion Criteria: - Creatinine clearance < 60mL/min - Platelet count below the normal reference - Coagulation (PT/PTT) tests above the normal reference - Any prior use of PrEP - Use of PEP within 30 days prior to study entry - Receipt of - anti-coagulant medications (e.g. warfarin). Aspirin is allowable. - Systemic corticosteroid medications - Non-steroidal anti-inflammatory drug (NSAID) use >2 days/week - Signs or symptoms of acute HIV infection within 14 days of study entry - No availability of another person who will drive participant home on days of entry and follow-up procedures. - Plan to leave the Seattle area in the subsequent 2.5 months - Any condition or substance use that, in the opinion of the study investigator, would interfere with study participation.


NCT ID:

NCT02621242


Primary Contact:

Principal Investigator
Joanne Stekler, MD
University of Washington


Backup Contact:

N/A


Location Contact:

Seattle, Washington 98104
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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