Comparative study of the effects of two oral contraceptive pills containing Drospirenone (3mg) with 30 mcg of ethinyl oestradiol and 20 mcg of ethinyl oestradiol, in polycystic ovary syndrome.

DRSUDHINDRA MOHAN BHATTACHARYA0 sites80 target enrollmentTBD

ConditionsHealth Condition 1: null- POLYCYSTIC OVARY SYNDROME

Overview

Phase: 未知
Intervention: Not specified
Conditions: Health Condition 1: null- POLYCYSTIC OVARY SYNDROME
Sponsor: DRSUDHINDRA MOHAN BHATTACHARYA
Enrollment: 80
Status: Recruiting
Last Updated: 4 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

4 years ago

Study Type

Interventional

Investigators

Sponsor

DRSUDHINDRA MOHAN BHATTACHARYA

Eligibility Criteria

Inclusion Criteria

•women with oligomenorrhoea diagnosed as having Polycystic ovary syndrome as per the Rotterdam criteria 2003; age\- minimum gynaecological age of 3 years(age since menarche) to 35 years

Exclusion Criteria

•secondary causes of hyperandrogenism like gross hypothyroidism, hyperprolactinaemia, Cushing syndrome, late onset congenital adrenal hyperplasia, contraindications of oral pill therapy,severe liver/ renal/cardiac disease; those already taken oral pills in the preceding 3 months.

Outcomes

Primary Outcomes

Not specified

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