Health Condition 1: null- Polycystic Ovarian Syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Women in the reproductive age group with Polycystic ovarian syndrome (PCOS), according to Rotterdam criteria 2.Willing to participate in study and follow up
Exclusion criteria
Exclusion criteria: • Patient already on other drugs for treatment of PCOS like Oral Contraceptive Pills • Deranged kidney or liver function tests • Uncontrolled Thyroid disorders or Hyperprolactinemia • Known hypersensitivity to metformin or myoinositol/ D-Chiro-inositol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| primary end point in this study will be-post prandial endogenous insulin levelsTimepoint: primary end point in this study will be-post prandial endogenous insulin levels | — |
Secondary
| Measure | Time frame |
|---|---|
| A. Improvement in clinical parameter includes 1. menstrual cycle irregularity 2. BMI 3. Waist : Hip ratio 4. Hirsutism/acne B. Improvement in Metabolic and hormonal parameters includes 1. Lipid profile 2. Blood sugar fasting and post prandial 3. Insulin fasting and post prandial 4. Glucose to insulin ratio 5. LH/FSH ratio 6. Serum Testosterone 7. DHEAS 8. HOMA IR IndexTimepoint: At the end of 6 months | — |
Countries
India
Contacts
All India Institute of Medical Sciences Rishikesh