HIV Risk Reduction and Drug Abuse Treatment in Malaysia

Sponsor
Yale University (Other)
Overall Status
Completed
CT.gov ID
NCT00383045
Collaborator
National Institute on Drug Abuse (NIDA) (NIH)
180
2
52
90
1.7

Study Details

Study Description

Brief Summary

A randomized clinical trial comparing drug abuse and HIV risk reduction counseling (DC-HIV) alone, DC-HIV combined with naltrexone maintenance, and DC-HIV combined with buprenorphine maintenance for the treatment of heroin addicts in Malaysia.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Combining drug abuse and HIV risk reduction counseling with opioid agonist maintenance treatment (OMT) or antagonist maintenance treatment with naltrexone (NMT) is effective for reducing illicit drug use and preventing HIV transmission associated with heroin dependence, but support for NMT and OMT remains tenuous in many Western Pacific countries (e.g., Malaysia, Indonesia and Singapore) where heroin addiction and HIV infection are epidemic and closely linked due to injection drug use (IDU) and high-risk sexual behaviors among addicts. Promising results of NMT in Malaysia have created interest in evaluating OMT using buprenorphine (BMT) and comparing the efficacy of counseling alone and counseling combined with BMT or NMT. This 24-week, randomized double blind clinical trial compares the efficacy for preventing heroin use and relapse and reducing HIV risk behaviors of manual-guided, HIV risk reduction and drug counseling (DC-HIV) alone or when combined with buprenorphine maintenance treatment (BMT) or naltrexone maintenance treatment (NMT) for recently detoxified and currently abstinent heroin dependent patients (N=180) in Malaysia (Specific Aim 1). The study will allow evaluation of 3 hypotheses: DC-HIV plus naltrexone is superior to DC-HIV alone; DC-HIV plus buprenorphine is superior to DC-HIV alone; and DC-HIV plus naltrexone is superior to DC-HIV plus buprenorphine. Primary outcome measures, assessed by 3x/wk urine toxicology testing and self-report, include resumption of heroin use, 1 or 3 weeks continuous relapse and reductions in HIV risk behaviors. The project will also evaluate the characteristics of treatment-seeking heroin addicts in Malaysia (including specific risk behaviors and patterns of HIV risk behaviors; prevalence of psychiatric and other medical comorbidity; and patterns of social, family, vocational, and criminal activity and service needs-Specific Aim 2). This data will be used to revise the DC-HIV manual to address the specific circumstances and risk behaviors of Malaysian heroin addicts. Finally, the project provides clinical training for health professionals and training and mentoring in drug abuse treatment and HIV prevention research to clinical researchers who will continue development, implementation, evaluation and dissemination of HIV prevention and drug abuse treatment approaches in Malaysia after the project ends (Specific Aim 3). The results of the study will inform government policy and support for HIV prevention and drug abuse treatment efforts in Malaysia and possibly also in other Western Pacific countries.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Double
Primary Purpose:
Treatment
Official Title:
HIV Risk Reduction and Drug Abuse Treatment in Malaysia
Study Start Date :
Apr 1, 2003
Actual Study Completion Date :
Aug 1, 2007

Outcome Measures

Primary Outcome Measures

  1. Time to resumption of heroin use []

  2. Time to relapse []

  3. Maximum consecutive weeks of opiate abstinence []

  4. Reduction of HIV risks []

Secondary Outcome Measures

  1. Addiction-related functional status []

  2. Adverse events []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Opioid dependence
Exclusion Criteria:
  • Dependence on alcohol, benzodiazepines or sedatives

  • Suicide or homicide risk

  • Psychotic disorder or major depression

  • Inability to read or understand the protocol or assessment questions

  • Life-threatening or unstable medical problems

  • Greater than 3 times normal liver enzymes (AST, GGT)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Yale University School of Medicine New Haven Connecticut United States 06519
2 Substance Abuse Research Center Muar Johor Malaysia

Sponsors and Collaborators

  • Yale University
  • National Institute on Drug Abuse (NIDA)

Investigators

  • Principal Investigator: Richard S. Schottenfeld, M.D., Yale University
  • Study Director: Mahmud Mazlan, M.D., Hospital Muar, Malaysia

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00383045
Other Study ID Numbers:
  • 0103012336
  • R01DA014718-04
First Posted:
Oct 2, 2006
Last Update Posted:
Mar 31, 2020
Last Verified:
Feb 1, 2009

Study Results

No Results Posted as of Mar 31, 2020