Ultrasound-guided Fascia Iliaca Compartment Block Versus Periarticular Infiltration

Completed · Not applicable

Conditions studied: Postoperative Pain

In brief

This randomized, controlled, observer-blinded study clinical trial was designed to evaluate ultrasound-guided fascia iliaca compartment block with ropivacaine and periarticular infiltration with ropivacaine for postoperative pain management after total hip arthroplasty.

Key facts

Study ID

NCT02658240

Run by

University of Texas Southwestern Medical Center

People needed

60

Starts

2016-04-05

Expected to finish

2017-12-16

Last updated by the study team

2018-11-29

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Female ASA physical status 1-3 scheduled for total hip arthroplasty
• Age 18-80 years old
• Able to participate personally or by legal representative in informed consent in English or Spanish

You may not qualify if…

• History of relevant drug allergy
• Age less than 18 or greater than 80 years
• Chronic opioid use or drug abuse
• Significant psychiatric disturbance
• Inability to understand the study protocol
• Refusal to provide written consent

Where it is running

• UTSW Parkland Health Hospital System — Dallas, Texas, United States

Full record on ClinicalTrials.gov

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