Smoking Clinical Trial
Official title:
Combined Nortriptyline and Transdermal Nicotine for Smoking Cessation
Treatment of smokers with a tricyclic antidepressant, nortriptyline, can reduce tobacco withdrawal symptoms and increases long term cessation rates when combined with transdermal nicotine and a behavioral cessation programs. The study is a placebo-controlled, randomized, parallel group trial in which smokers aged 18-70 will be subject to the combination of oral and patch treatments.
Status | Completed |
Enrollment | 158 |
Est. completion date | January 2003 |
Est. primary completion date | December 2002 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Aged 18-70, - smoking > 10 cigarettes per day, - no current major depression, - no concurrent psychiatric medications Exclusion Criteria: |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | VA Eastern Colorado Health Care System, Denver | Denver | Colorado |
Lead Sponsor | Collaborator |
---|---|
VA Office of Research and Development |
United States,
Prochazka AV, Kick S, Steinbrunn C, Miyoshi T, Fryer GE. A randomized trial of nortriptyline combined with transdermal nicotine for smoking cessation. Arch Intern Med. 2004 Nov 8;164(20):2229-33. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Validated smoking cessation | 6 months | No |
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---|---|---|---|
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