Effectiveness of Mifepristone and Misoprostol V/S Misoprostol alone in the induction of labor- a Randomised Controlled Trial
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2023/06/053518
- Lead Sponsor
- Dr Sneha Chakraborty
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria:
1) Women with Ultrasonographically confirmed Singleton pregnancy of 37-42weeksduration
2) Cephalic presentation
3) No contraindications to vaginal delivery
4) Post dated pregnancies
5) Reactive FHR
6) Bishop score <6
7) Rh negative pregnancies
8) Intact membranes
Exclusion Criteria:
1. Previous Lower Segment Cesarean Section (LSCS). 2. Intra Uterine Growth Restriction (IUGR). 3. Oligohydramnios. 4. Malpresentation. 5. Associated medical disorder
(hypertension, diabetes mellitus, heart disease, anemia, thyroid, epilepsy, asthma). 6. Premature Rupture of Membrane (PROM). 7. Congenital Anomaly. 8. Hypersensitivity to Prostaglandins & Mifepristone. 9. Preeclampsia, Eclampsia. 10. Placental insufficiency. 11. Cephalo Pelvic Disproportion. 12. Patient not willing to participate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Objective â?? To determine the effectiveness of mifepristone and misoprostol V/S misoprostol alone in induction of labor.Timepoint: 1 year
- Secondary Outcome Measures
Name Time Method Secondary Objective â?? To determine the feto maternal outcome in both the groups.Timepoint: 1 year