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EXPAREL Facia Iliaca Compartment Block for Intertrochanteric Hip Fracture — RESTORE  

Hip Fractures Clinical Trial

Official title:
A Phase-4, Multicenter, Randomized, Active-Controlled Study to Evaluate the Efficacy and Safety of EXPAREL When Administered Via Fascia Iliaca Compartment Block Versus Fascia Iliaca Compartment Block With Continuous Infusion of Ropivacaine Per Standard of Care Through a Catheter in Intertrochanteric Hip Fracture Patients

Clinical Trial Summary

This study evaluates the effect of EXPAREL on total opioid consumption through 72 hours following fascia iliaca compartment block (FICB) in subjects undergoing repair of intertrochanteric hip fracture.

Clinical Trial Description

The current standard of care treatment for pain relief in patients with intertrochanteric hip fracture is a FICB with continuous infusion of ropivacaine given via catheter.

In this study, some people will receive a single injection FICB with EXPAREL + bupivacaine HCl. The groups will be evaluated to determine the amount of pain medication they took from the FICB to 72 hours after. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03955458
Study type Interventional
Source Pacira Pharmaceuticals, Inc
Contact
Status Withdrawn
Phase Phase 4
Start date August 26, 2019
Completion date May 2020
View Details
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