Induction of labour with balloon catheter or balloon catheter with controlled-release dinoprostone vaginal insert
Not Applicable
Completed
- Conditions
- Induction of labour in nulliparous women at termPregnancy and Childbirth
- Registration Number
- ISRCTN12282883
- Lead Sponsor
- Obstetric and gynecology department , UMMC
- Brief Summary
2022 Results article in https://pubmed.ncbi.nlm.nih.gov/34999923/ (added 10/01/2022)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 206
Inclusion Criteria
1. Nulliparous women (no previous pregnancy beyond 20 weeks of gestation)
2. Unfavourable cervix (Bishop score =5)
3. Aged 18 years or older
4. =37 weeks of gestation at enrolment
5. Singleton birth
6. Cephalic presentation
7. Membrane intact
8. Normal pre-induction CTG (cardiotocography)
9. Contraction not more than 2:10
Exclusion Criteria
1. Gross fetal anomaly
2. Allergy to latex or dinoprostone
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <br> 1. Interval between the start of induction and vaginal delivery as recorded in patient medical records<br> 2. Maternal satisfaction with the birth experience from induction of labour to delivery assessed using<br> a numerical rating scale. A Likert scale will be used to determine whether the patient would recommend the method they had for induction of labour to a friend who needs to undergo induction of labour. This assessment will be done as soon as practicable after delivery.<br>
- Secondary Outcome Measures
Name Time Method