CompletedNot Applicable

Fetal Pillow Randomized Controlled Trial

United States60 participantsStarted 2018-01-13

Plain-language summary

The purpose of this study is to evaluate outcomes following cesarean delivery for failure to progress with the use of the Fetal Pillow. Our hypothesis is that time to delivery of the fetus is shorter with implementation of the Fetal Pillow.

Who can participate

Age range18 Years – 50 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * women age 18-50 * term pregnancy (37- 41 6/7 weeks) * singleton gestation in cephalic presentation * fully dilated * both nulliparous and multiparous women * both spontaneous labor and labor inductions Exclusion Criteria: * breech presentation * presence of contraindication to vaginal delivery * prior cesarean section * presence of congenital anomalies

What they're measuring

Uterine incision to delivery time

Timeframe: Assessed at time of delivery, delivery day (day 0)

Trial details

NCT IDNCT03342508

SponsorBrigham and Women's Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-08-01

View on ClinicalTrials.gov More Labor Complication trials