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Tobacco Cessation in Postmenopausal Women (Part II) - 2

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status and phase

Completed
Phase 1

Conditions

Tobacco Use Disorder

Treatments

Drug: Nicotrol

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00061074
R01DA008075-02 (U.S. NIH Grant/Contract)
NIDA-08075-2

Details and patient eligibility

About

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

Enrollment

1 patient

Sex

Female

Ages

40 to 79 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Double Blind

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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