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Membrane Stripping for Cervical Ripening | Clinical Trials | Clareo Health

RECRUITINGNA

Membrane Stripping for Cervical Ripening

Evaluation of Stripping for Cervical Ripening - A Randomized Controlled Study

NCT06591247•Meir Medical Center

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.

Eligibility

Age

18 - 50 years

Sex

FEMALE

Healthy Volunteers

Yes

Inclusion Criteria

•Patients aged 18 and above
•Patients with a cervical dilation of at least 1 cm
•Full-term pregnancy
•Cephalic presentation
•No contraindication to vaginal delivery

Exclusion Criteria

•Patients with rupture of membranes
•Patients who do not require cervical ripening and proceed directly to the delivery room for induction with oxytocin
•Patients for whom the use of a double-balloon catheter is contraindicated
•Twin pregnancies
•Pregnancies with macrosomic fetuses where vaginal delivery is contraindicated
•Vaginal deliveries after a cesarean section
•Patients with maternal or fetal pathologies that do not allow for vaginal delivery due to concerns about fetal or maternal distress

Locations (1)

Meir Medical Center

Kfar Saba, Central District, Israel

Key Dates

Start Date

August 7, 2024

Primary Completion Date

December 31, 2026

Completion Date

December 31, 2026

Last Updated

September 19, 2024

Enrollment

200

ESTIMATED participants

Conditions

Labor, InducedCervical RipeningBalloon InductionMembrane StrippingPregnancy Related

Interventions

Double Baloon Catheter

DEVICE

Membrane Stripping

PROCEDURE

Contacts

Gal Cohen, MD

CONTACT

+972545915788 galcwork@gmail.com

Combined Nipple Stimulation and Foley Balloon for Cervical Ripening

NCT07317674

Induction of LaborCervical Ripening

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COMPLETEDNA

Latent Phase Membrane Stripping for Caesarean Section Reduction

NCT06809985

Cesarean DeliveryCervical Ripening+1 more

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: September 19, 2024Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Membrane Stripping for Cervical Ripening

Inclusion Criteria

Exclusion Criteria

Combined Nipple Stimulation and Foley Balloon for Cervical Ripening

Latent Phase Membrane Stripping for Caesarean Section Reduction

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Comparing Methods for Balloon Catheter Inserting: View Guided (Speculum) Versus Manual Guided at Cervical Examination

Cervical Ripening: A Comparison Between Intravaginal Misoprostol Tablet and Intracervical Foley's Catheter and Subsequent Induction of Labor, Safety and Efficacy in Federal Teaching Hospital Abakaliki, Ebonyi State, Nigeria.