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Clinical Trial Summary

Using a randomized double-blinded study design, the study goal is to evaluate the superiority of Erector Spinae Plane block (ESPB) in the peri-operative pain management of patients undergoing surgery through a flank or anterior subcostal incision as compared to the standard of care of using IV and oral opiates.


Clinical Trial Description

40 subjects will be randomized in to 2 groups, with 20 in each group. - Group 1. Erector spinae plane block (ESPB) (containing Ropivacaine) - Group 2. Sham Erector spinae plane block. (SESPB) (with normal saline) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03691935
Study type Interventional
Source Milton S. Hershey Medical Center
Contact
Status Enrolling by invitation
Phase Phase 4
Start date September 28, 2018
Completion date February 28, 2025

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