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Clinical Trial Summary

The objective of our study is to evaluate the effect of CPAP on umbilical cord acid base status in morbidly obese women at the time of scheduled cesarean delivery. We hypothesize that neonates born to mothers wearing CPAP during the cesarean section will have a higher umbilical artery pH.


Clinical Trial Description

This is a randomized control trial comparing CPAP to routine airway management in morbidly obese patients undergoing scheduled cesarean delivery. Morbidly obese women meeting criteria for inclusion will be approached for participation. Women who are scheduled for cesarean delivery at Sentara Norfolk General Hospital will be approached at a prenatal appointment prior to scheduled date of delivery. If a woman agrees to participate in the study, she will be counseled and consented at that time. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04993651
Study type Interventional
Source Eastern Virginia Medical School
Contact Kristin Ayers, MPH
Phone 7574460579
Email ayerskl@evms.edu
Status Recruiting
Phase N/A
Start date October 11, 2021
Completion date August 31, 2022

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