Comparison on patient satisfaction with Cervical Ripening Balloon using inpatient and outpatient protocol

Not Applicable

• Conditions: Obstetrics: induction of labour; Pregnancy and Childbirth; Labour

• Registration Number: ISRCTN10109823
• Lead Sponsor: ational Maternity Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-05-29
• Study Completion: 2020-01-31
• Last Update Posted: 24 August 2020

Recruitment & Eligibility

• Status: Stopped
• Sex: Female
• Target Recruitment: 40

Inclusion Criteria

1. Nulliparous women with singleton pregnancies
2. Aged 18 to 40 years
3. The fetus is in cephalic presentation
4. Low risk pregnancies going for induction of labour for postdates pregnancies as per protocol in National Maternity Hospital

Exclusion Criteria

1. Any pre-existing medical condition or medical condition of pregnancy
2. Pathological CTG prior to induction
3. Oligohydramnios or any other abnormal findings on post-dates scan
4. Maternal age <18 years old or >40 years old

Study & Design

• Study Type: Interventional
• Study Design: Not specified