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Naltrexone Augmentation of Nicotine Patch Therapy - 1

Tobacco Use Disorder Clinical Trial

Official title:
Naltrexone Augmentation of Nicotine Patch Therapy

Clinical Trial Summary

Naltrexone Augmentation of Nicotine Patch Therapy

Clinical Trial Description

This double blind placebo controlled study is designed to determine whether naltrexone can be used to help reduce cigarette use and craving for cigarettes. Eligible participants will receive 21mg transdermal nicotine as an outpatient. In addition, participants will receive one of three doses of naltrexone (25,50 or 100mg) or a placebo and brief counseling over the course of six weeks with follow-up appointments three, six, and twelve months after the beginning of treatment. ;

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00218153
Study type Interventional
Source National Institute on Drug Abuse (NIDA)
Contact
Status Completed
Phase Phase 3
Start date November 2000
Completion date April 2004
View Details
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