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Simple nipple stimulation may shorten labor for induced births

NCT ID NCT07317674

Symptom relief Sponsor: Western Galilee Hospital-Nahariya Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether adding nipple stimulation to a standard balloon catheter can help ripen the cervix and shorten the time from induction to delivery. About 100 pregnant women at term with an unfavorable cervix will be randomly assigned to receive either the balloon plus nipple stimulation or the balloon alone. The goal is to see if this simple, natural method can improve outcomes and reduce the need for additional interventions.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Jan 2028

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Pregnant individuals aged ≥18 years * Singleton pregnancy * Term gestation (37-42 weeks) * Cephalic fetal presentation * Intact membranes * Bishop score \<6 at enrollment * Medical indication for labor induction Exclusion Criteria: * Multiple gestation * Previous cesarean delivery or uterine surgery * Contraindication to vaginal delivery * Major fetal anomalies * Active labor at enrollment * Unstable fetal lie or presentation * Contraindication to Foley balloon catheter insertion * Conditions precluding nipple stimulation (e.g., local breast infection, prior breast surgery involving the nipple)

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Cervical ripening Induction of labor

How to take part

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