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Ethinyl Estradiol and Cyproterone Acetate in Irregular Menstruation

Dysmenorrhea Clinical Trial

Official title:
Phase IV Study of the Use of Two Preparations of Ethinyl Estradiol and Cyproterone Acetate in Irregular Menstruation of Hyper-androgenic Origin

Clinical Trial Summary

This is a Phase IV, randomized, double-blind, comparative study of the use of two preparations of ethinyl estradiol and cyproterone acetate in the treatment of menstrual irregularities of hyper-androgenic origin.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01103518
Study type Interventional
Source Fundação Educacional Serra dos Órgãos
Contact
Status Active, not recruiting
Phase Phase 4
Start date December 2009
Completion date January 2011
View Details
See also
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