Adaptive Pharmacotherapy for Smoking Cessation
Summary
The purpose of this study is to assess an "adaptive" approach to smoking cessation pharmacotherapy. The protocol is designed to compare adaptive vs. standard approaches to two common smoking cessation pharmacotherapies - Varenicline (commonly known as Chantix) and the Nicotine Patch. The investigators hypothesize that participants allocated to adaptive therapy will show significantly higher biochemically confirmed 30-day continuous abstinence at 12 weeks post-Target Quit Day (TQD).
Timeline
- Start
- 2017-06-06
- Primary completion
- 2020-07-30
- Completion
- 2021-05-12
Outcome
Met primary endpoint
paper 23 of 95 participants (24%) in the adaptive treatment group and 8 of 93 participants (9%) in the standard treatment PMID 37682573 ↗
paper (odds ratio [OR], 3.38; 95% CI, 1.43-7.99; P = .004) PMID 37682573 ↗
paper This randomized clinical trial found that adaptive pharmacotherapy was efficacious for smoking cessation treatment in a practice setting. PMID 37682573 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bupropion | Small molecule | — | — |
| Subject | Nicotine | Unknown | — | — |
| Subject | Varenicline | Small molecule | — | — |