Regional Anesthesia in Hip Arthroscopy

Withdrawn before enrolling · Not applicable · Has a placebo group

Conditions studied: Femoroacetabular Impingement

In brief

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.

Key facts

Study ID

NCT02674113

Run by

University of Missouri-Columbia

People needed

0

Starts

2015-10-01

Expected to finish

2017-10-01

Last updated by the study team

2017-02-10

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patient undergoing primary hip arthroscopy with labral repair and osteoplasty for hip impingement
• Age 18-45 years old
• Not pregnant
• No history of neuropathic pain
• No radiographic signs of osteoarthritis of the operative hip (Tönnisgrade 1)
• Willing and able to comply with post-operative hip arthroscopy protocol
• No documented allergy to anesthetic agents
• Able to attend follow up appointments

You may not qualify if…

• Allergy to regional anesthetic
• Age <18 or >45 years
• Pregnant females
• History of neuropathic pain
• Radiographic signs of osteoarthritis (Tönnis grade 2)
• Unable to speak/understand English
• Currently imprisoned
• Unwilling/unable to provide consent

Where it is running

• University of Missouri Health System — Columbia, Missouri, United States

Full record on ClinicalTrials.gov

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