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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00564252
Other study ID # 84-5-6886
Secondary ID IUMS127
Status Completed
Phase N/A
First received November 26, 2007
Last updated November 26, 2007
Start date February 2006
Est. completion date October 2006

Study information

Verified date November 2007
Source Iran University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ethics Committee
Study type Interventional

Clinical Trial Summary

the purpose of this study is to evaluate the efficacy of topical Finasteride in the treatment of idiopathic hirsutism


Recruitment information / eligibility

Status Completed
Enrollment 56
Est. completion date October 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Idiopathic hirsutism which is defined as normal levels of androgens and normal ovulation

- Normal serum prolactin

Exclusion Criteria:

- Pregnancy

- Simultaneous use of other drugs for the treatment of hirsutism

Study Design

Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
topical finasteride
0.2%topical(cream)finasteride twice a day for six months

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Iran University of Medical Sciences Firuzgar hospital affiliated to Iran University of Medical Sciences

Outcome

Type Measure Description Time frame Safety issue
Primary the efficacy of topical finasteride was determined by comparison of Ferriman-Gallwey score before and after medication 6 months
Secondary the efficacy of topical finasteride was determined by comparison of mean hair thickness before and after medication 6 months