Combined Nipple Stimulation and Foley Balloon for Cervical Ripening

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorWestern Galilee Hospital-Nahariya

About this trial

Labor induction rates have increased substantially worldwide, and successful cervical ripening remains a key determinant of induction outcomes. Mechanical cervical ripening with a Foley balloon catheter is widely used and considered safe, while nipple stimulation promotes endogenous oxytocin release and represents a physiologic method for stimulating uterine contractions. However, the combined effect of nipple stimulation and balloon catheter use has not been systematically evaluated.

This prospective, randomized, double-blinded controlled trial will assess whether the addition of nipple stimulation to Foley balloon catheter cervical ripening improves Bishop score and shortens the induction-to-delivery interval compared with balloon catheter alone. Term pregnant patients (37-42 weeks' gestation) with a singleton, cephalic pregnancy and an unfavorable cervix (Bishop score \<6) requiring labor induction will be randomized to receive either Foley balloon catheter plus standardized nipple stimulation or Foley balloon catheter alone.

The primary outcomes are change in Bishop score after catheter removal and time from catheter insertion to delivery. Secondary outcomes include need for additional induction methods, mode of delivery, maternal and neonatal outcomes, pain, patient satisfaction, and breastfeeding rates. The study aims to evaluate the efficacy and safety of incorporating a physiologic intervention into standard mechanical cervical ripening.

Eligibility criteria

Qualifiers

Pregnant individuals aged ≥18 years

Singleton pregnancy

Term gestation (37-42 weeks)

Cephalic fetal presentation

Disqualifiers

Multiple gestation

Previous cesarean delivery or uterine surgery

Contraindication to vaginal delivery

Major fetal anomalies

Trial design

Treatments tested in this trial

  • Foley balloon catheter with nipple stimulation
  • Mechanical cervical ripening with Foley catheter

Treatment groups

100 Participants
are divided into 2 treatment groups

Locations

This trial has no locations