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Clinical Trials/IRCT20080929001281N3
IRCT20080929001281N3
Completed
Phase 3

A randomized clinical trial to compare the effectiveness of oral contraceptives containing levonorgestrel, desogestrel, cyproterone acetate, and drospirenone on levels of adipokines, and adiposity indices in women with polycystic ovary syndrome.

Shahid Beheshti University of Medical Sciences0 sites80 target enrollmentTBD
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Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Shahid Beheshti University of Medical Sciences
Enrollment
80
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Existence of diagnostic criteria for polycystic ovary syndrome based on Androgen Excess and PCOS Society (AES)
  • •Age range: 18 to 45 years

Exclusion Criteria

  • •Use of hormonal; anti\-androgen or insulin sensitizer drugs for at least 3 months before the study
  • •Detection of severe hypertension; chronic disease; recent surgery or diagnosis of cancer
  • •Appearing the serious side effects such as thrombosis

Outcomes

Primary Outcomes

Not specified

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