drugset / Trial / NCT00344695

Bupropion Treatment for Youth Smoking Cessation

NCT00344695 ↗

Phase 3 Completed University of Arizona
RandomizedSingle-groupDouble-blindTreatment

Summary

The purpose of this study is to 1) evaluate the safety and efficacy of two doses of bupropion SR (150mg/day and 300mg/day) when compared to placebo, as an aid to smoking cessation in adolescents and 2) to examine which factors, such as medication adherence, nicotine dependence, and motivation to quit, affect treatment outcome.

Timeline

Start
—
Primary completion
—
Completion
2003-04

Outcome

Met primary endpoint

paper Cotinine-confirmed 7-day point prevalence abstinence rates at 6 weeks were as follows: placebo, 5.6%; 150 mg, 10.7%; and 300 mg, 14.5% (P = .03, 300 mg vs placebo). PMID 17984409 ↗

paper Sustained-release bupropion hydrochloride, 300 mg/d, plus brief counseling demonstrated short-term efficacy for adolescent smoking cessation. PMID 17984409 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Bupropion Small molecule 150 mg —
Subject Bupropion Small molecule 300 mg —

Indications