A clinical trial to study the effects of an oral pill containing desogestrel in women with polycystic ovary syndrome.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- EFFECTS ON CLINICAL PARAMETERS - BMI, ABDOMINAL CIRCUMFERENCE, HIRSUTISM, ACNE, BLOOD PRESSURETESTOSTERONE, SHBG, FAI VALUE, FASTING GLUCOSE: INSULIN RATIO.
- Registration Number
- CTRI/2009/091/000370
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
women with polycystic ovary syndrome , diagnosed as per Rotterdam 2003 criteria
Exclusion Criteria
secondary causes of hyperandrogenism; those already on oestrogenic preparations in the preceding three months; hypothyroidism, hyperprolactinaemia, women with severe liver diseases, renal diseases, cardiac diseases.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method