Could a breast pump kickstart labor?

NCT ID NCT07588529

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
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By invitation only
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Paused for now. It may or may not start again.
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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 Results may not be published yet.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)

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Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
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First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether using a breast pump for nipple stimulation can safely start labor in pregnant women. The gentle suction may trigger the body's own oxytocin to encourage contractions. Researchers will measure total labor time and compare it to standard methods. The goal is to give patients more control and possibly shorten delivery.

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 48 people

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

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Dec 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

Ages

18 to 50 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: All patients presenting to KUMC labor \& delivery for IOL will be considered for this study. Maternal * ≥18 years old and ≤ 50 years old * ≥37wga and ≤ 42wga * Intact amniotic membranes * English speaking Fetal * Cephalic presentation Exclusion Criteria: Maternal * Inability to give informed consent * History of cesarean delivery or uterine myomectomy * History of uterine rupture * Intrahepatic cholestasis of pregnancy * Maternal life-threatening conditions * Active HSV * Gestational hypertension, Preeclampsia (severe or w/o severe features), HELLP, chronic hypertension on medications Placental * Placenta previa, vasa previa * Suspicion for abnormally adherent placenta * Chorioamnionitis * Placental abruption Fetal * Multifetal gestation * category 2 or 3 fetal heart tracing upon presentation (does not include isolated variable deceleration) * EFW \> 5000 grams in mother with diabetes * EFW \> 4500 grams in mother without diabetes * Fetal demise * Fetal growth restriction \<10th centile * Any other contraindication for vaginal birth or anticipation of need for NICU for care of baby

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How to take part

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  2. The official record

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Contacts and locations

Locations

  • University of Kansas Medical Center

    Kansas City, Kansas, 66103, United States

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