Pre to Postoperative Smoking Cessation

Stopped early · Phase 2

Conditions studied: Cigarette Smoking, Obesity

In brief

The study will evaluate the feasibility of integrating an intensive pre- post-surgical smoking cessation intervention into a hospital setting, and assess measures of postsurgical recovery as a function of smoking cessation status.

Key facts

Study ID

NCT02683161

Run by

Johns Hopkins University

People needed

5

Starts

2015-10-01

Expected to finish

2017-07-01

Last updated by the study team

2018-07-17

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Smoker who has surgery scheduled 5-10 weeks in advance

You may not qualify if…

• being contraindicated for varenicline use
• evidence of psychiatric instability
• being unwilling/unable to adhere to the study schedule
• be unwilling to provide study access to medical records
• being otherwise judged by the study team to be inappropriate for study participation

Where it is running

• Johns Hopkins Bayview Medical Center — Baltimore, Maryland, United States

Full record on ClinicalTrials.gov

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