Clinical trial to compare the effectiveness of Kulathachoorna Udvarthana followed by Ardhamatrika Vasthi and Conventional Allopathic management in Polycystic ovary syndrome of Overweight women.
Phase 3
- Conditions
- Health Condition 1: E663- OverweightHealth Condition 2: E282- Polycystic ovarian syndrome
- Registration Number
- CTRI/2023/02/050074
- Lead Sponsor
- Central Council for Research in Ayurvedic Sciences CCRAS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Females diagnosed by the presence of any two of the three Rotterdam criteria(Oligomenorrhea, clinical evidence of hyperandrogenism, Polycystic ovaries by ultrasonography)
BMI 25.0-29.9
Participants who have given informed consent Participants eligible for vasthi.
Exclusion Criteria
Participants suffering with conditions like Congenital adrenal hyperplasia, Androgen secreting tumors, Thyroid disorders, Cushing syndrome, Diagnosed cases of other Endocrine disorders, Elevated Prolactin levels,
Participants under steroid therapy
Participants under antipsychotics
Pregnant and lactating mothers
Patients with evidence of malignancy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in Menstrual Interval <br/ ><br>Change in Menstrual DurationTimepoint: At 0th day and after treatment(90th day)
- Secondary Outcome Measures
Name Time Method Change in number and size of cysts <br/ ><br>Change in BMI <br/ ><br>Change in Waist circumference <br/ ><br>Change in Waist-hip ratio <br/ ><br>Change in Serum Insulin levels <br/ ><br>Change in QOL scoresTimepoint: At 0th day and after treatment(90th day)