Actively Recruiting
Post Analytic Treatment Interruption Study
Led by SEARCH Research Foundation · Updated on 2026-04-27
100
Participants Needed
1
Research Sites
782 weeks
Total Duration
On this page
Sponsors
S
SEARCH Research Foundation
Lead Sponsor
U
US Military HIV Research Program
Collaborating Sponsor
AI-Summary
What this Trial Is About
This exploratory study is designed to ensure the safety of HIV-infected volunteers who complete research protocols that include an analytic treatment interruption (ATI). This is a prospective cohort study of volunteers who were diagnosed with HIV during early acute HIV infection, treated with antiretroviral therapy (ART) and subsequently enrolled in a clinical study that included ATI. After completion of study participation that involves ATI, participants will be recruited into this study for continued clinical and laboratory monitoring.
CONDITIONS
Official Title
Post Analytic Treatment Interruption Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Man or woman aged 60;18 years.
- Enrolled in RV254 study.
- Completed clinical research protocol that included ATI within one month of enrollment in this protocol.
- Able and willing to provide written informed consent or witnessed verbal informed consent with thumbprint if illiterate.
- Able to participate in study visits for up to 144 weeks.
- Willing to have photo or fingerprint taken for identification purposes.
- Female-specific: agrees not to become pregnant while not receiving ART. If sexually active without hysterectomy, tubal ligation, or menopause, must agree to abstinence, prescription birth control, or barrier birth control while off ART.
You will not qualify if you...
- History of medical or psychiatric condition that could jeopardize safety or rights, interfere with protocol adherence, or ability to give informed consent.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
SEARCH
Bangkok, Bangkok, Thailand, 10330
Actively Recruiting
Research Team
S
Somchai Sriplienchan, MD, MPH
CONTACT
N
Nitiya Chomchey, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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