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Completed

NCT Number: NCT03089983

Addiction, HIV and Tuberculosis in Malaysian Criminal Justice Settings

The purpose of this study is to conduct empiric studies of tuberculosis (TB) among people in prison with and without a history of opioid dependence. A RCT of latent TB infection prevention strategies among HIV+ and HIV- prisoners with high prevalence of hepatitis C (HCV) using standard 40-week daily isoniazid (40H) vs short-course weekly isoniazid + rifapentine (12HR). Investigators will also use this data, and publicly available data to complete agent-based modeling for comparative and cost-effectiveness of various TB screening and treatment strategies among prisoners.

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Key information

About this study

Screening: All newly admitted prisoners (80-120 new inmates on admission days) undergo a complete assessment, including a brief exam and mandatory rapid HIV test by the prison medical unit. Each prisoner waiting to be evaluated will be invited for participation in TB screening activities (not currently part of standard care). If they verbally assent to wanting to learn more in a group session, their names and ID will be recorded and then invited for informed consent privately, followed by a brief survey, WHO symptom assessment, tuberculin skin testing (TST) with reading after 72 hours, sputum induction on 2 consecutive mornings for AFB smear, TB culture (results back 6-8 weeks using the BACTEC MGIT 960 liquid culture gold standard), and point-of care (POC) Gene Xpert. Each person will have phlebotomy for HBV and HCV Ab, LFTs, and if HIV+, CD4 testing (all of these are POC using Alere™). For those with CD4<50, they will undergo POC low-cost, urinary TB-LAM lateral flow testing (sensitivity=67%) (Alere™ Determine) to identify disseminated TB. Additional demographic, drug use, and TB risks will also be assessed along with prison data (release date, previous incarcerations, type of offense). Participants will then undergo CXR testing. A TB specialist will review all patients and results, ensuring that patients with suspected TB initiate treatment. All suspected or confirmed cases active TB cases in HIV+ prisoners will have ART initiated after 2 weeks of TB treatment initiation (if CNS TB not suspected) if CD4<50 and within 8 weeks for all others.

Trial: All HIV+ and HIV- prisoners with latent TB infection (LTBI) (TST reaction 10 mm or greater) from screening will be asked to participate in the trial. Enrolled participants will undergo block stratified randomization, stratifying on three factors: a) CD4<350; b) HCV Ab status; and c) ART status. After randomization and allocation to 12HR or 40H, participants will be provided 12HR weekly (12 weeks) and INH daily (26 weeks) as directly observed therapy. Every 4 weeks, patients will be monitored for AST/ALT and adverse side effects. Premature treatment discontinuation will occur for any DAIDS Grade 4 toxicity or patient refusal to continue.

The focus of this registration is the RCT. Outcomes measures were updated to match most recent protocol March 2025.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Inclusion criteria

(screening):

  • Age ≥ 18 years
  • Newly admitted inmate at Kajang Prison

Inclusion criteria

(Trial):

  • Age ≥ 18 years HIV-1 seropositivity
  • Confirmed LTBI (TST ≥ 5mm if HIV+; TST ≥ 10 mm if HIV-)
  • Meets DSM-V criteria for opioid dependence
  • >9 months before release (to ensure treatment completion in prison)
  • AST/ALT < 3x upper limit normal

Exclusion criteria

  • Unable to provide informed consent
  • On a protease inhibitor
  • Women who are pregnant or are planning on becoming pregnant

Treatment and study plan

Isoniazid

Drug

Participants will be randomized to receive standard INH as TB preventative treatment

rifapentine

Drug

Participants will be randomized to receive short course INH + RIF as TB preventative treatment

Primary outcomes

  1. TB Treatment Completion Rates in Prison

    Time frame: 3 to 6 months

    TB treatment completion in prison will be verified using medical records. All TB treatment in prison will be administered under directly observed therapy (DOTs), and treatment administration will be recorded in the participant's prison medical record. Data presented here is the number of participants that completed TB treatment of those that initiated treatment.

Secondary outcomes

  1. TB Treatment Adherence

    Time frame: monthly for up to 6 months

    TB treatment adherence in prison will be verified using medical records. All TB treatment in prison will be administered under directly observed therapy (DOTs), and treatment administration will be recorded in the participant's prison medical record. Data presented here is the number of participants that adhered to TB treatment of those that initiated treatment.

  2. Discontinuation Due to Experiencing an Adverse Event

    Time frame: up to 6 months

    The number of participants that discontinued the trial due to experiencing an Adverse Event

  3. Acceptability of Starting the Trial

    Time frame: Day 1

    Acceptability defined as the number of eligible participants that agreed to consent

Sponsors and collaborators

Lead sponsor

Yale University

Other

Collaborators

  • National Institute on Drug Abuse (NIDA)
  • University of Malaya

Registry information

Acronym: HARAPAN II

Important dates

Study start
2017
Primary completion
2024
Study completion
2024
First posted
Mar 24, 2017
Registry last updated
Feb 9, 2026

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.

Published trials that share one or more normalized conditions with this study.