Observational
OtherHPTN 073 is an observational study in MSM in the United States
NCT Number: NCT01808352
Black men who have sex with men (MSM) Pre-Exposure Prophylaxis (PrEP) Study with Client Centered Care Coordination (C4) Component.
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Notify Me18 year and older
Male
Observational
UCLA Vine Street Clinic, Los Angeles, California, United States
An open label demonstration study with PrEP and Client Centered Care Coordination (C4) to assess the initiation, acceptability, safety, and feasibility of PrEP for Black MSM (BMSM) in three US Cities. A subset of participants will also be recruited to participate in qualitative interviews about facilitators and barriers regarding PrEP. The study will recruit HIV-uninfected BMSM at risk for HIV infection in three US Cities. Enrollment will include those aged 18 and over with an effort to recruit an equal number of BMSM under age 25 and over age 25 with a total of 225 participants (75 per site).
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
BMSM who meet all of the following criteria are eligible for inclusion in this study:
i. Receptive or insertive anal intercourse with more than three male sex partners ii. Exchange of money, gifts, shelter or drugs for receptive or insertive anal sex with a male partner iii. Receptive or insertive anal sex while under the influence of drugs or alcohol (i.e., high or drunk within two hours of the sex act) according to self-report"
o eCcr in mL/min = [(140 - age in years) x (actual body weight in kg)] / (72 x serum creatinine in mg/dL) Alanine aminotransferase (AST) and aspartate aminotransferase (ALT) < 3 times the upper limit of normal (ULN)
Exclusion criteria
BMSM who meet any of the following criteria will be excluded from this study:
HPTN 073 is an observational study in MSM in the United States
Time frame: 30 months
Documented in either study CRFs or ACASI
Time frame: 30 months
Adherence will be assessed via self-report (ACASI), PBMCs and plasma concentration
Time frame: 30 months
Graded via DAIDS Toxicity Grading System determined by review of reported adverse events (clinical and laboratory)
Time frame: 30 months
Rectal and urine GC/CT, and NAAT for syphilis and chlamydia
Time frame: 30 months
Measured by ACASI assessments
Time frame: 30 months
Refusal rates will be measured by ACASI assessments
Time frame: 30 months
HIV RNA and genotyping will be performed at the NL on samples confirmed to be HIV infected
Time frame: 30 months
Assessed via interviewer-administered questionnaire
HIV Prevention Trials Network
Network
Pre-Exposure Prophylaxis (PrEP) Initiation and Adherence Among Black Men Who Have Sex With Men (BMSM) in Three U.S. Cities
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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