Efficacy and safety for women and their unborn babies using misoprostol as a vaginal insert to induce labour for women past 40 weeks of pregnancy
Phase 4
Completed
- Conditions
- Induction of labour in women with prolonged pregnanciesPregnancy and Childbirth
- Registration Number
- ISRCTN14702259
- Lead Sponsor
- utheran-Protestant Hospital (EVK)
- Brief Summary
2020 Preprint results in https://doi.org/10.21203/rs.3.rs-70051/v1 (added 04/03/2022)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 304
Inclusion Criteria
1. Aged over 18 years
2. No prior history of Caesarean section
3. Prolonged pregnancy requiring induction of labour
Exclusion Criteria
Contraindications for prostaglandins
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <br> Measured using case report forms:<br> 1. Time from insertion to the onset of labour (hours)<br> 2. Time from onset of labour until delivery (hours)<br> 3. Time from insertion to birth was measured (hours)<br>
- Secondary Outcome Measures
Name Time Method There are no secondary outcome measures