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NCT00040040 Clinical Trial

Assessment of Potential Interactions Between Methamphetamine and Bupropion - 1

Amphetamine-Related Disorders Clinical Trial

Official title:
Double-Blind, Placebo-Controlled Assessment of Potential Interactions Between IV Methamphetamine and Oral Bupropion

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00040040
Other study ID # NIDA-CTO-0010-1
Secondary ID
Status Active, not recruiting
Phase Phase 1
First received June 18, 2002
Last updated January 10, 2017
Start date June 2002
Est. completion date September 2003

Study information
Verified date August 2003
Source National Institute on Drug Abuse (NIDA)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess potential interactions between intravenous (IV) methamphetamine and oral bupropion.

Description:

This is a human laboratory clinical pharmacology study to assess potential interactions between IV methamphetamine challenge and treatment with oral sustained-release bupropion.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 20
Est. completion date September 2003
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

Please contact site director for more details.

Exclusion Criteria:

Please contact site director for more details.

Study Design

Allocation: Randomized, Masking: Double-Blind, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Intervention

Drug:
• Bupropion

Locations
Country Name City State
United States University of Texas Health Science Center Houston Texas
United States UCLA Integrated Substance Abuse Program Los Angeles California

Sponsors (2)
Lead Sponsor Collaborator
National Institute on Drug Abuse (NIDA) University of California, Los Angeles

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Psychological effects
Primary BP, HR
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