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Clinical Trial Summary

This study will investigate the effect of three types of wound infiltration on post Cesarean opioid analgesia consumption when used in conjunction with an opioid free postoperative analgesia pathway.


Clinical Trial Description

The subjects that meet the inclusion criteria of the study will be randomized preoperatively into three arms following a 1:1:1 ratio. During the intraoperative course one of three combinations of wound infiltration will be administered to subjects prior to the closure of the surgical incision. Subjects in Group I will receive a placebo of normal saline. Subjects in Group II will receive bupivacaine alone. Subjects in Group III will receive both bupivacaine and dexmedetomidine. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03545516
Study type Interventional
Source Richmond University Medical Center
Contact Nisha Lakhi, MD
Phone 718-818-2109
Email NLAKHI@RUMCSI.org
Status Not yet recruiting
Phase Phase 2
Start date September 17, 2018
Completion date November 1, 2018

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