Varenicline Light Smoking Pilot

2019-09-19 03:56:38 | BioPortfolio


The goal of this study is to assess varenicline vs. placebo for its effect on decreasing cue reactivity in light and intermittent smokers.


The study will consist of randomization to receive either varenicline or placebo over 6 weeks and include 5 study visits. Participants are offered an optional additional 6 weeks of active varenicline. Cue reactivity will be assessed in both a lab-based setting (viewing series of images and rating cravings) and in a real-world setting (text-based daily interaction).

Study Design


Smoking Cessation


Varenicline, Placebo oral tablet


Duke University
North Carolina
United States


Not yet recruiting


Duke University

Results (where available)

View Results


Published on BioPortfolio: 2019-09-19T03:56:38-0400

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