Is Nipple Stimulation Effective for Inducing Labor and Acceptable to Patients, Nurses, and Providers?

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorUniversity of Kansas Medical Center

About this trial

In this study the investigators will be testing the use of the Symphony PLUS® breast pump for nipple stimulation. Typically, breast pumps are used to start breast milk production and collect breast milk in patients after delivering their baby. The device uses cup-shaped pieces called flanges that are placed over the patient's nipples and then a gentle vacuum or suction is applied. The mechanical effect of the suction on the nipple is thought to cause the release of a substance called oxytocin in one's body, which encourages labor and contractions to begin. Some reasons why nipple stimulation might be better than other induction of labor methods are that it allows the patient to have more control over their induction process, it uses the patient's own oxytocin instead of synthetic (or factory-produced) oxytocin, and it may shorten the time that it takes to deliver the baby.

Eligibility criteria

Qualifiers

≥18 years old and ≤ 50 years old

≥37wga and ≤ 42wga

Intact amniotic membranes

English speaking Fetal

Disqualifiers

Inability to give informed consent

History of cesarean delivery or uterine myomectomy

History of uterine rupture

Intrahepatic cholestasis of pregnancy

Trial design

Treatments tested in this trial

  • Electric breast pump for nipple stimulation
  • induction of labor

Treatment groups

48 Participants
are divided into 2 treatment groups