Could a breast pump kickstart labor?
NCT ID NCT07588529
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.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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About 48 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 50 years
- Sex
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Female participants only
- Healthy volunteers
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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 Hide 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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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Kansas Medical Center
Kansas City, Kansas, 66103, United States
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