Regional Anesthesia in Hip Arthroscopy

Status Withdrawn

Clinical Trial Summary

The purpose of this research is to determine differences in outcomes in patients who receive regional anesthesia (a fascia iliaca block) versus placebo prior to undergoing hip arthroscopy with labral repair and/or debridement and osteoplasty for hip impingement.

Clinical Trial Description

Methods: After informed consent is obtained at a routine/pre-surgical clinic visit, all patients who meet eligibility criteria will undergo randomization into one of two groups. These groups are 1) to receive regional anesthesia (a single shot fascia iliaca block using bupivacaine) prior to hip arthroscopy, or 2) undergo a subcutaneous injection procedure using a normal saline placebo (0.9% sodium chloride in water) instead of bupivacaine. Intra-operatively, both groups will receive general anesthesia and local anesthesia (lidocaine and bupivacaine in the peripheral compartment). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02674113
Study type	Interventional
Source	University of Missouri-Columbia
Contact
Status	Withdrawn
Phase	N/A
Start date	October 2015
Completion date	October 2017

View Details

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