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Sponsors and Collaborators: |
National Institute on Drug Abuse (NIDA) University of Texas |
Information provided by: | National Institute on Drug Abuse (NIDA) |
ClinicalTrials.gov Identifier: | NCT00000307 |
The purpose of this study is to evaluate naltrexone as an adjunct in alcoholic cocaine dependent patients; concurrent relapse prevention theory.
Condition | Intervention | Phase |
Alcohol-Related Disorders Cocaine-Related Disorders |
Drug: Naltrexone |
Phase II |
Drug Information available for: | Naltrexone 8-Azabicyclo(3.2.1)octane-2-carboxylic acid, 3-(benzoyloxy)-8-methyl-, methyl ester, (1R-(exo,exo))- Cocaine hydrochloride Naltrexone hydrochloride |
Study Type: | Interventional |
Study Design: | Treatment |
Official Title: | Naltrexone as an Adjunct in Alcoholic Cocaine Dependent Patients |
Estimated Enrollment: | 0 |
Study Start Date: | April 2003 |
Study Completion Date: | April 2007 |
Primary Completion Date: | April 2007 (Final data collection date for primary outcome measure) |
Ages Eligible for Study: | 18 Years to 50 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Please contact site for information.
United States, Texas | |||||
University of Texas Health Science Center | |||||
Houston, Texas, United States, 77225 |
National Institute on Drug Abuse (NIDA) |
University of Texas |
Principal Investigator: | John Grabowski, Ph.D. | University of Texas |
Responsible Party: | University of Texas Medical School at Houston ( Joy Schmitz, Ph.D. ) |
Study ID Numbers: | NIDA-09262-4, P50-09262-4 |
First Received: | September 20, 1999 |
Last Updated: | August 11, 2008 |
ClinicalTrials.gov Identifier: | NCT00000307 |
Health Authority: | United States: Federal Government |
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