Clinical Study To Assess The Efficacy of Ayurvedic Formulations In PCOS
- Conditions
- Health Condition 1: N830- Follicular cyst of ovary
- Registration Number
- CTRI/2020/07/026410
- Lead Sponsor
- ational Institute of Ayurveda Jaipur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Patients willing to give voluntary informed consent.
Both married and unmarried patients.
ASRM/ESHRE (Rotterdam) Criteria,2013- Affected individuals must have two out of three criteria
1. Oligo and /or anovulation
2. Hyperandrogenism (clinical and /or biochemical).
3. Polycystic ovaries(Confirmed on USG).
Patients not willing to give voluntary informed consent.
Women of age <18years and >40years.
Patients with chronic systemic illness (Congestive cardiac failure, Hypertension, cirrhosis of liver, chronic renal disease, diabetes mellitus, Tuberculosis etc.).
Patients using oral contraceptive pills.
Patients with any organic reproductive system abnormalities (Excluded clinically and radiologically), pelvic inflammatory disease, hydrosalpinx, endometriosis, adenomyosis, fibroid uterus, carcinoma of reproductive organ.
Any type of malignancy.
Patients with positive Sexually transmitted diseases (STDs), Human Immunodeficiency Virus HIV, Hepatitis B Surface Antigen(HbsAg).
Patients suffering from adrenal hyperplasia, severe insulin resistance, androgen secreting neoplasm, thyroid abnormalities, Cushingâ??s syndrome.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in features of oligomenorrhoea /anovulation.Timepoint: 3 months
- Secondary Outcome Measures
Name Time Method Changes in PCOS features (i.e. acne, hirsutism).Timepoint: 3 months