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Completed Phase 2 Interventional Results available

Phase 2, Double-Blind, Placebo-Controlled Trial of Bupropion for Methamphetamine Dependence

ClinicalTrials.gov ID: NCT00687713

Public ClinicalTrials.gov record NCT00687713. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 1:03 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is to assess the efficacy of bupropion in reducing methamphetamine use in subjects with methamphetamine dependence who report using methamphetamine 29 or less days during the 30 days prior to the start of signing consent.

Study identification

NCT ID
NCT00687713
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
200 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2008 (Type not available)
Primary completion
May 2011 (Actual)
Completion
May 2011 (Actual)
Last update posted
Mar 21, 2017

2008 – 2011

United States locations

U.S. sites
12
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
UCLA Integrated Substance Abuse Program Los Angeles California 90025 —
South Bay Treatment Center San Diego California 92115 —
Addiction and Pharmacology Research Laboratory San Francisco California 94110 —
Friends Research Institute Torrance California 90502 —
Matrix Institute Woodland Hills California 91364 —
Pacific Addiction Research Center - U of Hawaii Honolulu Hawaii 96817 —
Iowa Luther Hospital Des Moines Iowa 50316 —
U of Kansas Medical Center Kansas City Missouri 64131 —
New York University New York New York 10010 —
Medical University of South Carolina Charleston South Carolina 29425 —
University of Texas Health Science At San Antonio San Antonio Texas 78229-3900 —
VA Salt Lake City Health Care System Salt Lake City Utah 84148 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00687713, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 21, 2017 · Synced Oct 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00687713 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →