drugset / Trial / NCT00717093

Study Evaluating The Efficacy Of Varenicline In Cessation Of Oral Smokeless Tobacco Use

NCT00717093 ↗

Phase 4 Completed 432 enrolled Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary goal of this study is to compare efficacy of varenicline to placebo for cessation of use of smokeless tobacco.

Timeline

Start
2008-08
Primary completion
2009-04
Completion
2009-07

Outcome

Met primary endpoint

registry Varenicline Tartrate vs Placebo; p <0.0001; Odds Ratio (OR) 2.39 (95% CI 1.59 to 3.58) NCT00717093 ↗

paper Continuous abstinence rate at week 9-12 was higher in the varenicline group than the placebo group PMID 21134997 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Varenicline Small molecule 1 mg —

Indications