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NCT00061074 Clinical Trial

Tobacco Cessation in Postmenopausal Women (Part II) - 2

Tobacco Use Disorder Clinical Trial

Official title:
The Effects of ERT on Appetitive Behavior and Withdrawal in Short-term Smoking Cessation in Postmenopausal Females on Transdermal Nicotine Replacement

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00061074
Other study ID # NIDA-08075-2
Secondary ID R01DA008075-02
Status Completed
Phase Phase 1
First received May 21, 2003
Last updated December 1, 2015
Start date March 1993
Est. completion date March 2000

Study information
Verified date December 2015
Source University of Minnesota - Clinical and Translational Science Institute
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 1
Est. completion date March 2000
Est. primary completion date March 2000
Accepts healthy volunteers No
Gender Female
Age group 40 Years to 79 Years
Eligibility 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.

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Nicotrol

Locations
Country Name City State
United States University of Minnesota Minneapolis Minnesota

Sponsors (2)
Lead Sponsor Collaborator
University of Minnesota - Clinical and Translational Science Institute National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

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