drugset / Trial / NCT00364156

Comparison of Standard Versus Extended Nicotine Patch Therapy for Smoking Cessation

NCT00364156 ↗

RandomizedParallel-groupDouble-blindTreatment

Summary

This randomized double-blind, placebo-controlled will determine the relative efficacy of standard versus extended transdermal nicotine (TN) therapy for smoking cessation. After completing the eligibility screening, 600 treatment-seeking smokers will be randomized to receive either standard treatment (ST) with TN (21mg x 8 weeks, placebo x 16 weeks) or extended treatment (ET) with TN (21mg x 24 weeks). All participants will receive behavioral counseling. The primary outcome will be biochemically verified abstinence from smoking at the end of treatment (week 24). Secondary outcomes include abstinence at week 28 (4 weeks after treatment is discontinued), and time to failure. We hypothesize that ET will produce significantly higher quit rates than ST; however, the benefit of ET will last only so long as treatment is continued. Support for this hypothesis would indicate that maintenance therapy with TN should be considered.

Timeline

Start
2004-06
Primary completion
2008-04
Completion
2008-05

Outcome

Mixed primary results

paper At week 24, extended therapy produced higher rates of point-prevalence abstinence (31.6% vs. 20.3%; odds ratio, 1.81 [95% CI, 1.23 to 2.66]; P = 0.002) PMID 20124230 ↗

paper At week 52, extended therapy produced higher quit rates for prolonged abstinence only (P = 0.027). PMID 20124230 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Nicotine Unknown 21 mg Other

Indications