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Study identifier: NCT06591247 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Membrane Stripping for Cervical Ripening

Condition: Labor, Induced · Cervical Ripening · Balloon Induction  ·  Sponsor: Meir Medical Center

PhaseNA
Planned participants400
Who can joinFemale, 18 Years to 50 Years
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Gal Cohen, MD  ·  +972545915788  ·  galcwork@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Meir Medical CenterKfar Saba, Central District, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT06591247