Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00539123 · ClinicalTrials.gov registry record · NA

Drug Counseling and Abstinent-Contingent Take-Home Buprenorphine in Malaysia

A NA study, sponsored by Yale University.

Completed
Registry status
NA
Development phase
234
Enrollment target

NCT00539123 is a NA study that has completed, run by Yale University. The registered enrollment target is 234 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00539123, a NA study, has completed, sponsored by Yale University.

COMPLETED
Registry status
NA
Development phase
234 participants
Enrollment target

Study Summary

A randomized clinical trial evaluating whether Behavioral Drug and HIV Risk Reduction Counseling (BDRC), abstinence-contingent take-home buprenorphine (ACB), or the combination of the two improve efficacy and cost-effectiveness of standard buprenorphine treatment for opiate-dependent individuals in Malaysia.

Interventions

  • BEHAVIORAL behavioral drug and HIV risk reduction counseling (BDRC)
  • BEHAVIORAL abstinence-contingent buprenorphine (ACB)

Trial Details

FieldValue
Enrollment Target 234 participants
Start Date 2007-09
Est. Completion 2012-08
Phase NA

Sponsor

Yale University

1,492 total trials

What the Registry Record Tells You About NCT00539123

The ClinicalTrials.gov registry entry for NCT00539123 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 234 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Yale University, which has 1,492 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which behavioral drug and HIV risk reduction counseling (BDRC) is the first listed.

NCT00539123 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00539123 about?

NCT00539123 is a clinical study titled "Drug Counseling and Abstinent-Contingent Take-Home Buprenorphine in Malaysia". A randomized clinical trial evaluating whether Behavioral Drug and HIV Risk Reduction Counseling (BDRC), abstinence-contingent take-home buprenorphine (ACB), or the combination of the two improve efficacy and cost-effectiveness of standard buprenorphine treatment for opiate-dependent individuals in ...

What is the current status of trial NCT00539123?

This trial is currently completed. It is a NA study. The enrollment target is 234 participants. The study started on 2007-09. Estimated completion is 2012-08.

What interventions are being tested in trial NCT00539123?

The interventions under investigation include: behavioral drug and HIV risk reduction counseling (BDRC) (BEHAVIORAL), abstinence-contingent buprenorphine (ACB) (BEHAVIORAL).

Who is sponsoring clinical trial NCT00539123?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.