About this trial

The reported risk of nonreassuring fetal heart trace following neuraxial analgesia is 3-23%. This variability may be due to fluid and oxytocin management prior to and during the initiation of neuraxial analgesia. The study hypothesis is that decreasing the oxytocin infusion rate by 50 % prior to initiation of combined spinal epidural analgesia will cause a reduction in the incidence of adverse fetal heart rate changes.

Eligibility criteria

Qualifiers

Healthy nulliparous or multiparous women at term (37 > weeks' gestation)

Singleton pregnancy

Request for neuraxial analgesia

Oxytocin used for induction of labor or augmentation of labor per institutional protocols

Disqualifiers

Use of chronic analgesic medications

Prior administration of systemic opioid labor analgesia

Non-vertex presentation

Contraindication to neuraxial analgesia

Trial design

Treatments tested in this trial

  • Half dose Oxytocin

Treatment groups

730 Participants
are divided into 2 treatment groups

Locations

2
University of Iowa Hospitals and Clinics52245, Iowa CityIowa, United States
Medical College of Wisconsin53226, MilwaukeeWisconsin, United States

Sponsors and collaborators

Unyime Ituk

Lead sponsor

University of Iowa

Sponsor institution