Tobacco Cessation in Postmenopausal Women (Part II) - 2

This study has been completed.
Sponsor:
Information provided by:
National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov Identifier:
NCT00061074
First received: May 21, 2003
Last updated: June 23, 2005
Last verified: May 2003

May 21, 2003
June 23, 2005
March 1993
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Complete list of historical versions of study NCT00061074 on ClinicalTrials.gov Archive Site
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Tobacco Cessation in Postmenopausal Women (Part II) - 2
The Effects of ERT on Appetitive Behavior and Withdrawal in Short-Term Smoking Cessation in Postmenopausal Females on Transdermal Nicotine Replacement

The purpose of this study is to evaluate the effects of ERT on appetitive behavior and withdrawal in short-term smoking cessation in postmenopausal females on transdermal nicotine replacement

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Interventional
Phase 1
Allocation: Randomized
Masking: Double-Blind
Primary Purpose: Treatment
Tobacco Use Disorder
Drug: Nicotrol
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
0
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Inclusion Criteria:

(Same as Part I)

Exclusion Criteria:

Same as Part I, with the addition of those who have had a past reaction to transdermal nicotine patch or have active skin diseases will be excluded.

Female
40 Years to 79 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00061074
NIDA-08075-2, R01-08075-2
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National Institute on Drug Abuse (NIDA)
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Principal Investigator: Sharon Allen, Ph.D., M.D. University of Minnesota - Clinical and Translational Science Institute
National Institute on Drug Abuse (NIDA)
May 2003

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP