Topical Finasteride in the Treatment of Idiopathic Hirsutism

NCT ID: NCT00564252

Last Updated: 2007-11-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

56 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-02-28

Study Completion Date

2006-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Idiopathic Hirsutism

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

topical finasteride

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

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Firuzgar hospital affiliated to Iran University of Medical Sciences

OTHER

Sponsor Role collaborator

Iran University of Medical Sciences

OTHER

Sponsor Role lead

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

iraj heydari, professor assistant

Role: STUDY_DIRECTOR

endocrine and metabolism centre of Iran University of Medical Sciences

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

IUMS127

Identifier Type: -

Identifier Source: secondary_id

84-5-6886

Identifier Type: -

Identifier Source: org_study_id