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NCT00856323 · ClinicalTrials.gov registry record · Phase 2

Contingency Management for Methamphetamine Abstinence and HIV Post-Exposure Prophylaxis in Men Who Have Sex With Men

A Phase 2 study of HIV Infections and HIV, sponsored by Friends Research Institute.

Completed
Registry status
Phase 2
Development phase
53
Enrollment target
1
Study location

NCT00856323 is a Phase 2 study of HIV Infections and HIV that has completed, run by Friends Research Institute. The registered enrollment target is 53 participants, below the 446-participant average among 542 other HIV Infections trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00856323, a Phase 2 study of HIV Infections and HIV, has completed, sponsored by Friends Research Institute.

COMPLETED
Registry status
Phase 2
Development phase
53 participants
Enrollment target
1
Study location

Study Summary

This study seeks to decrease methamphetamine use and concomitant high-risk sexual behaviors among methamphetamine-using men who have sex with men (MSM) by combining a biomedical intervention with a behavioral intervention. The behavioral intervention will consist of an 8-week course of contingency management (CM) through which participants will be reinforced for testing negative for methamphetamine metabolites during periodic urine analyses. The biomedical intervention involves a 28-day course of an antiretroviral drug (Truvada) to be administered after an unanticipated HIV risk exposure (i.e., engaging in either receptive or insertive anal sex without a condom with someone who is HIV-positive or of unknown status). In combining these two interventions, this study seeks to evaluate the combined intervention's effects on sexual risk behaviors and methamphetamine use.

Interventions

  • DRUG Truvada
  • BEHAVIORAL CM

Study Locations (1)

California

  • Friends Community Center - Los Angeles

Trial Details

FieldValue
Enrollment Target 53 participants
Start Date 2009-01
Est. Completion 2010-12
Phase Phase 2

Sponsor

Friends Research Institute

41 total trials

What the Registry Record Tells You About NCT00856323

The ClinicalTrials.gov registry entry for NCT00856323 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 53 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 446-participant average among 542 other HIV Infections trials with a reported enrollment target (88% lower). The listed sponsor is Friends Research Institute, which has 41 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with HIV Infections appearing as the primary indexed condition, and to 2 interventions - of which Truvada is the first listed.

NCT00856323 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT00856323 about?

NCT00856323 is a clinical study titled "Contingency Management for Methamphetamine Abstinence and HIV Post-Exposure Prophylaxis in Men Who Have Sex With Men". This study seeks to decrease methamphetamine use and concomitant high-risk sexual behaviors among methamphetamine-using men who have sex with men (MSM) by combining a biomedical intervention with a behavioral intervention. The behavioral intervention will consist of an 8-week course of contingency m...

What is the current status of trial NCT00856323?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 53 participants. The study started on 2009-01. Estimated completion is 2010-12.

What conditions does trial NCT00856323 study?

This clinical trial studies the following conditions: HIV Infections, HIV, Amphetamine-Related Disorders.

What interventions are being tested in trial NCT00856323?

The interventions under investigation include: Truvada (DRUG), CM (BEHAVIORAL).

Who is sponsoring clinical trial NCT00856323?

This trial is sponsored by Friends Research Institute, which has 41 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00856323 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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.