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Clinical Trials/TCTR20170408001
TCTR20170408001
Recruiting
未知

Effectiveness and Cost Effectiveness of a Combination HIV Preventive Intervention with and without daily oral Truvada® pre-exposure prophylaxis (PrEP) with adherence support among young men who have sex with men (YMSM) and transgender women (TGW) ag

S National Institutes of Health (NIH)0 sites1,240 target enrollmentApril 8, 2017

Overview

Phase
未知
Intervention
Not specified
Conditions
HIV Infection Prevention
Sponsor
S National Institutes of Health (NIH)
Enrollment
1240
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 8, 2017
End Date
October 10, 2020
Last Updated
last year
Study Type
Interventional
Sex
Male

Investigators

Sponsor
S National Institutes of Health (NIH)

Eligibility Criteria

Inclusion Criteria

  • •Biological male sex at birth
  • •Self\-report of having sold or traded sex to another man for money, drugs, or other goods or services in the previous 12 months.
  • •Age 18 through 26 years at enrollment
  • •Self\-reported living in the greater Bangkok Metropolitan area or Pattaya City
  • •Willing to complete study instruments, with or without assistance, Thai and/or English.
  • •Thai citizenship
  • •Willing to provide contact and locator information
  • •Self\-reported negative or unknown HIV status
  • •Negative rapid HIV test result at the screening visit

Exclusion Criteria

  • •Unable or unwilling to provide consent for study participation
  • •Rapid HIV test results at the screening visit suggesting HIV infection
  • •Did not complete baseline assessment (Section 3\.1 above)
  • •Any condition that would make participation in the study unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.
  • •Concurrently enrolled in another PrEP (oral or topical or injectable) intervention trial or preventive HIV vaccine trial.

Outcomes

Primary Outcomes

Not specified

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