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Membrane Stripping for Cervical Ripening

Study acronym: Stripping
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Enrollment target: 200 to 400v2 Show 5 more changesShow less
    • Primary and study completion dates: Dec 31, 2026 to Dec 31, 2027
    • Interventions: Double Baloon Catheter (Device), Membrane Stripping (Procedure) to Double Baloon Catheter (Device), Membrane Stripping (Procedure), PGE2 (Drug)
    • Eligibility criteria shortened, about 6 words
    • Site contact updated
    • Study arms: 2 to 3
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this interventional study is to evaluate the effectiveness of membrane stripping in cervical ripening compared to double balloon catheter induction. The study population consists of women undergoing labor induction. The main questions it aims to answer are: 1. Is membrane stripping as effective as double balloon catheter induction in cervical ripening? 2. What is the influence of membrane stripping on the time required for cervical ripening, delivery duration, and maternal and fetal outcomes compared to balloon induction.
Trial Details
NCT Number NCT06591247
Lead Sponsor Meir Medical Center
Conditions
(from sponsor)		 Labor, Induced, Cervical Ripening, Balloon Induction, Membrane Stripping, Pregnancy Related, Induction of Birth
Enrollment 400 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov