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Clinical Trials/ISRCTN12282883
ISRCTN12282883Completed未知

Foley catheter vs Foley catheter and controlled-release dinoprostone insert labour induction in nulliparous women: a randomised trial

Obstetric and gynecology department , UMMC0 sites206 target enrollmentStarted: December 3, 2018Last updated:

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
206

Study Overview

Brief Summary

2022 Results article in https://pubmed.ncbi.nlm.nih.gov/34999923/ (added 10/01/2022)

Study Design

Study Type
Interventional

Eligibility Criteria

Sex
Female

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

Investigators

Sponsor
Obstetric and gynecology department , UMMC

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