A trial to see which form of the drug Misoprostol used for induction of labour is more effective and safer- in fluid form given at regular intervals starting at low dose or as a tablet with fixed dose.
Phase 4
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2023/03/051096
- Lead Sponsor
- Rajagiri Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. primigravida
2. 37-40 weeks of pregnancy
3. singleton pregnancy with cephalic presentation
4. no uterine scar
5. Bishop score less than or equal to 6
Exclusion Criteria
1.women with contraindications or hypersensitivity to misoprostol
2. women who do not consent to partiipate in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method