Optimization of Smoking Cessation Strategies Concurrent With Treatment of Tobacco Related Malignancies
NCT02048917 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 93
Last updated 2020-01-29
Summary
The purpose of this study is to find an optimal smoking cessation strategy in patients undergoing therapy for lung and head and neck cancers at selected cancer centers in Kentucky by delivering high quality smoking cessation to all enrolled patients. This study will also examine the feasibility of routinely implementing an array of smoking cessation strategies for this patient population.
Conditions
Interventions
- DRUG
-
High Intensity Counseling + Long Acting NRT + PRN NRT
High Intensity Counseling + Long Acting NRT + PRN NRT
- DRUG
-
High Intensity Counseling + bupropion + PRN NRT
High Intensity Counseling + bupropion + PRN NRT
- DRUG
-
High Intensity Counseling + varenicline + PRN NRT
High Intensity Counseling + varenicline + PRN NRT
- DRUG
-
High Intensity Counseling + Long Acting NRT
High Intensity Counseling + Long Acting NRT
- DRUG
-
High Intensity Counseling + bupropion
High Intensity Counseling + bupropion
- DRUG
-
High Intensity Counseling + varenicline
High Intensity Counseling + varenicline
- DRUG
-
Low Intensity Counseling + Long Acting NRT + PRN NRT
Low Intensity Counseling + Long Acting NRT + PRN NRT
- DRUG
-
Low Intensity Counseling + bupropion + PRN NRT
Low Intensity Counseling + bupropion + PRN NRT
- DRUG
-
Low Intensity Counseling + varenicline + PRN NRT
Low Intensity Counseling + varenicline + PRN NRT
- DRUG
-
Low Intensity Counseling + Long Acting NRT
Low Intensity Counseling + Long Acting NRT
- DRUG
-
Low Intensity Counseling + bupropion
Low Intensity Counseling + bupropion
- DRUG
-
Low Intensity Counseling + varenicline
Low Intensity Counseling + varenicline
Sponsors & Collaborators
-
Kentucky Lung Cancer Research Program
collaborator OTHER -
University of Kentucky
lead OTHER
Principal Investigators
-
Joseph Valentino, M.D. · University of Kentucky
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-07-22
- Primary Completion
- 2019-05-15
- Completion
- 2019-05-15
- FDA Drug
- Yes
Countries
- United States
Study Locations
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