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RECRUITING
NCT06591247
NA

Membrane Stripping for Cervical Ripening

Sponsor: Meir Medical Center

View on ClinicalTrials.gov

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.

Official title: Evaluation of Stripping for Cervical Ripening - A Randomized Controlled Study

Key Details

Gender

FEMALE

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

200

Start Date

2024-08-07

Completion Date

2026-12-31

Last Updated

2024-09-19

Healthy Volunteers

Yes

Interventions

DEVICE

Double Baloon Catheter

A double Baloon Catheter will be inserted for 12 hours to one of the arms of the study

PROCEDURE

Membrane Stripping

Stripping will be considered as 3-5 rotations of separating the amniotic sac from the cervix and will be perfomed twice (every 4-6 hours)

Locations (1)

Meir Medical Center

Kfar Saba, Central District, Israel