Fetal Pillow Randomized Controlled Trial

Completed · Not applicable

Conditions studied: Labor Complication

In brief

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.

Key facts

Study ID

NCT03342508

Run by

Brigham and Women's Hospital

People needed

60

Starts

2018-01-13

Expected to finish

2019-08-01

Last updated by the study team

2019-09-19

Who can join

Age: 18 and older, up to 50. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• breech presentation
• presence of contraindication to vaginal delivery
• prior cesarean section
• presence of congenital anomalies

Where it is running

• Brigham and Women's Hospital — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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