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NCT00018187 Clinical Trial

Combinations of Pharmacologic Smoking Cessation Treatments

Smoking Clinical Trial

Official title:
Combinations of Pharmacologic Smoking Cessation Treatments

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00018187
Other study ID # ADRD-011-98S
Secondary ID
Status Completed
Phase Phase 1
First received July 3, 2001
Last updated January 20, 2009
Start date November 1998
Est. completion date June 2001

Study information
Verified date May 2007
Source VA Office of Research and Development
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to test the effectiveness of a combination of the drugs bupropion and mecamylamine along with a nicotine patch as a therapy for smoking cessation.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date June 2001
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 40 Years
Eligibility Subjects must be a smoker between 20 and 40 years old, have smoked at least 20 cigarettes per day for at least 2 years, wish to stop smoking and be in good general health

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Bupropion

• Mecamylamine

• Nicotine Patch

Locations
Country Name City State
United States VA Greater Los Angeles Healthcare System Los Angeles California

Sponsors (1)
Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

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