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Addiction, HIV and Tuberculosis in Malaysian Criminal Justice Settings

Addiction, HIV and Tuberculosis in Malaysian Criminal Justice Settings

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03089983
Acronym
HARAPAN II
Enrollment
316
Registered
2017-03-24
Start date
2017-08-21
Completion date
2024-04-04
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Addiction, Hepatitis, HIV/AIDS, Opioid Dependence, Tuberculosis

Keywords

prison

Brief summary

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.

Detailed description

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.

Interventions

DRUGIsoniazid

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

DRUGRifapentine

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

Sponsors

Yale University
Lead SponsorOTHER
University of Malaya
CollaboratorOTHER
National Institute on Drug Abuse (NIDA)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
TB Treatment Completion Rates in Prison3 to 6 monthsTB 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

MeasureTime frameDescription
TB Treatment Adherencemonthly for up to 6 monthsTB 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.
Discontinuation Due to Experiencing an Adverse Eventup to 6 monthsThe number of participants that discontinued the trial due to experiencing an Adverse Event
Acceptability of Starting the TrialDay 1Acceptability defined as the number of eligible participants that agreed to consent

Countries

Malaysia

Contacts

PRINCIPAL_INVESTIGATORFrederick Altice, MD

Yale University

PRINCIPAL_INVESTIGATORAdeeba Kamarulzaman, MBBS

University of Malaya

PRINCIPAL_INVESTIGATORSheela Shenoi, MD

Yale University

Participant flow

Pre-assignment details

Of 327 eligible participants, 316 participants consented, 4 participants were excluded prior to randomization, and 312 randomized

Baseline characteristics

Characteristic
Age, Continuous42 years
Education level
Primary school and below
52 Participants
Education level
secondary school
100 Participants
Education level
Tertiary school
4 Participants
Elevated (>4) Alcohol Use Disorders Identification Test (AUDIT) C score18 Participants
Employed prior to incarceration119 Participants
Homelessness28 Participants
Marital Status
Married
33 Participants
Marital Status
Single/partner
180 Participants
Marital Status
Widowed/Divorced
34 Participants
Median Body Mass Index (BMI)21.51 kg/m²
Median days since prison entry76.5 days
Median number of prior incarcerations9 incarcerations
Number of Participants previously prescribed ART26 Participants
Positive Hepatitis C69 Participants
Positive Rapid Opioid Dependence Screen (RODS) (≥3) on enrollment112 Participants
Previous diagnosis of HIV17 Participants
Previous intravenous drug use (IVDU)67 Participants
Previously incarcerated294 Participants
Previously taking ART prior to prison entry6 Participants
Previous Opioid Use130 Participants
Previous TB disease10 Participants
Race/Ethnicity, Customized
Chinese
34 Participants
Race/Ethnicity, Customized
Indian
39 Participants
Race/Ethnicity, Customized
Malay
104 Participants
Race/Ethnicity, Customized
Other
1 Participants
Region of Enrollment
Malaysia
312 participants
Sex: Female, Male
Female
0 Participants
Sex: Female, Male
Male
156 Participants
Total people with HIV18 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 1560 / 156
other
Total, other adverse events
112 / 15684 / 156
serious
Total, serious adverse events
0 / 1560 / 156

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026