About this trial

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 criteria

Qualifiers

Patients aged 18 and above

Patients with a cervical dilation of at least 1 cm

Full-term pregnancy

Cephalic presentation

Disqualifiers

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/PGE2 is contraindicated

Twin pregnancies

Trial design

Treatments tested in this trial

  • Double Baloon Catheter
  • Membrane Stripping
  • PGE2

Treatment groups

400 Participants
are divided into 3 treatment groups

Locations

1
Meir Medical Center4428164, Kfar SabaCentral District, Israel

Sponsors and collaborators

Meir Medical Center

Lead sponsor