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Clinical Trial Summary

Labor patients who meet inclusion and exclusion criteria will be consented to be participate in this study to determine if the use of a peanut shaped birthing ball reduces the length of labor and reduces the incidence of cesarean section. Subjects will be randomized at the time of consent to either use the birthing ball or not use the birthing ball from the time of labor analgesia until complete cervical dilation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02539563
Study type Interventional
Source Wake Forest University Health Sciences
Contact
Status Terminated
Phase N/A
Start date June 4, 2015
Completion date December 26, 2017

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