- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00094289
Interactions Between Cocaine and Ethanol and Disulfiram - 1
January 10, 2017 updated by: National Institute on Drug Abuse (NIDA)
Interactions Between IV Cocaine and Ethanol and Oral Disulfiram
The purpose of this study is to assess potential interactions between intravenous cocaine and ethanol and oral disulfiram.
Study Overview
Status
Unknown
Intervention / Treatment
Detailed Description
This is a two-site, double blind, placebo-controlled inpatient study to determine the cardiovascular and psychiatric safety of alcohol use in cocaine-dependent subjects who had used cocaine after treatment with disulfiram.
Study Type
Interventional
Enrollment
16
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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California
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Los Angeles, California, United States, 90024
- UCLA Integrated Substance Abuse Program
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Texas
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San Antonio, Texas, United States, 78284 7828
- University of Texas Hlth Sci Ctr San Ant
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 50 years (ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Must meet DSM-4 criteria for cocaine abuse or dependence and are not seeking treatment.
- Ability to verbalize understanding of consent form and provide written informed consent and verbalize willingness to complete study procedures; be able to comply with protocol requirements.
Exclusion Criteria:
- Please contact site for more information.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
Safety assessments
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Psychological effects
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: John Roache, Ph.D., University of Texas Health Sci Cntr, San Antonio
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2004
Study Completion
July 1, 2005
Study Registration Dates
First Submitted
October 15, 2004
First Submitted That Met QC Criteria
October 14, 2004
First Posted (ESTIMATE)
October 15, 2004
Study Record Updates
Last Update Posted (ESTIMATE)
January 11, 2017
Last Update Submitted That Met QC Criteria
January 10, 2017
Last Verified
July 1, 2005
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NIDA-MDS-0003-1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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