Comparison Of Two Different Drugs For Hormone Replacement In Women With Premature Ovarian Insufficiency
Not Applicable
- Conditions
- Health Condition 1: N912- Amenorrhea, unspecified
- Registration Number
- CTRI/2020/07/026376
- Lead Sponsor
- Maulana Azad Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Women with premature ovarian insufficiency attending Gynaecology and Gynae- Endocrinology OPD in Lok Nayak Hospital.
Exclusion Criteria
1. Known allergies to the two progesterone preparations being studied.
2. Contraindicatin to use of hormone preparation- breast cancer, liver disease, thrombophilia.
3. patients with untreated hypothyroidism.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effect of two progesterone preparations on: <br/ ><br>1. Quality and duration of menstrual bleeding. <br/ ><br>2. Endometrial thickness on day 21(+/- 1 day) on USG.Timepoint: 1st, 2nd and 3rd month of each progesterone preparation.
- Secondary Outcome Measures
Name Time Method 1. Progesterone related subjective effects during the period of intake of the two progesterone preparations. <br/ ><br>2. Effect on lipid profile with two progesterone preparations. <br/ ><br>3. Patient satisfaction regarding their menstrual flow with the two progesterone preparations.Timepoint: At enrollment, at every month, and end of 3rd month of each progesterone preparation.