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Combined Nortriptyline and Transdermal Nicotine for Smoking Cessation



Combined Nortriptyline and Transdermal Nicotine for Smoking Cessation

For Condition: Smoking
Status: No longer recruiting
Sponsor(s): Department of Veterans Affairs Medical Research Service ,
Synopsis: 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.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Minimum Age/Maximum Age: 18 Years/70 Years
Genders: Both
Protocol Entry Criteria: - Aged 18-70, - smoking > 10 cigarettes per day, - no current major depression, - no concurrent psychiatric medications
Total Enrollment: 

Location and Contact Information:

VAMC
Denver,  Colorado,  80220
United States
 


Additional Information:
Study ID Numbers:
  ADRD-006-97F; 
Study Start Date: April 1998
Record last reviewed: June 2001
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00018148

Other Smoking Studies:
1. Behavioral Counseling for Alcohol Dependent Smokers (nicotine patch)

2. Combination Nicotine Replacement for Alcoholic Smokers

3. Behavioral/Drug Therapy for Alcohol-Nicotine Dependence (naltrexone/nicotine patch)

4. Naltrexone and Patch for Smokers

5. Timing of Smoking Intervention in Alcohol Treatment (nicotine patch)

Related Studies:

Other Smoking Clinical Trials
Other Colorado Clinical Trials
Other Denver Clinical Trials

Combined Nortriptyline and Transdermal Nicotine for Smoking Cessation

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