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Clinical Trial Summary

The purpose of this study is to evaluate the effect of non-dissecting the inferior rectus sheath during primary cesarean delivery on post-operative hemoglobin and post-operative pain control as measured by VAS score and opioid anesthesia use in the first 72 hours post-op.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02762773
Study type Interventional
Source University Hospital Case Medical Center
Contact David Sheyn, MD
Phone 513-225-2314
Email david.sheyn@uhhospitals.org
Status Not yet recruiting
Phase N/A
Start date September 2016
Completion date November 2017

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