Status:

UNKNOWN

Evaluation of Serum Prostatic Specific Antigen (PSA) After Cyproterone Compound Treatment Compared With Oral Contraceptives Pill in Hirsute Polycystic Ovary Syndrome Patients

Lead Sponsor:

Shahid Beheshti University

Conditions:

Polycystic Ovary Syndrome

Eligibility:

FEMALE

22-25 years

Phase:

PHASE2

PHASE3

Brief Summary

The purpose of this study is to evaluate the effect of oral contraceptive on the serum free prostatic specific antigen (PSA)in women with polycystic ovary syndrome(PCOD)compared with cyproterone compo...

Detailed Description

The purpose of this study is to evaluate the effect of oral contraceptive on the serum free prostatic specific antigen (PSA)in women with polycystic ovary syndrome(PCOD)compared with cyproterone compo...

Eligibility Criteria

Inclusion

  • PCOS patients

Exclusion

  • Women who received hormone therapy during the last 3 months,
  • On a diet
  • Herbal treatment
  • Hyperprolactinemia
  • Thyroid disorders
  • Ovarian tumors
  • Cushing disease.

Key Trial Info

Start Date :

February 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 1 2010

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT00955058

Start Date

February 1 2007

End Date

December 1 2010

Last Update

September 3 2009

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Taheripanah

Tehran, Tehran Province, Iran, 14137

Evaluation of Serum Prostatic Specific Antigen (PSA) After Cyproterone Compound Treatment Compared With Oral Contraceptives Pill in Hirsute Polycystic Ovary Syndrome Patients | DecenTrialz