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Tobacco Cessation in Postmenopausal Women (Part II) - 2

NCT00061074 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 1

Last updated 2015-12-02

No results posted yet for this study

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

Conditions

  • Tobacco Use Disorder

Interventions

DRUG

Nicotrol

Sponsors & Collaborators

Principal Investigators

  • Sharon Allen, Ph.D., M.D. · University of Minnesota

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Max Age
79 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
1993-03-31
Primary Completion
2000-03-31
Completion
2000-03-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00061074 on ClinicalTrials.gov