Study of oral Mifepristone as a cervical ripening agent to induce labour in low-risk full-term live pregnancy beyond 40 weeks of gestation.
Phase 4
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2024/02/062460
- Lead Sponsor
- maid Hospital, Dr SN Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Pregnant females of age between 18-45 years old, Primigravida or Gravida 2, with singleton live pregnancy with cephalic presentation of gestational age 40-41 weeks without any obstetric complications, having an unripe cervix and intact membranes.
Exclusion Criteria
Pregnant females having any obstetric complications, any previous uterine surgery, any fetal compromise.
Study & Design
- Study Type
- PMS
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method