Clinical Trial

Membrane Stripping for Cervical Ripening

Study acronym: Stripping
Recruiting
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Summary
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.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-09-07.
Trial Details
NCT Number NCT06591247
Lead Sponsor Meir Medical Center
Conditions Labor, Induced, Cervical Ripening, Balloon Induction, Membrane Stripping, Pregnancy Related, Induction of Birth
Enrollment 400 participants
Start Date 2024-08-07
Primary Completion 2027-12-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-04-15