Evaluating the Efficacy of Erector Spinae Block in Routine Hip Arthroscopy: A Prospective Analysis
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Hip Disease
- Sponsor
- Carilion Clinic
- Enrollment
- 120
- Locations
- 1
- Primary Endpoint
- Post Anesthesia Care Unit Pain
- Last Updated
- 4 years ago
Overview
Brief Summary
The aim of this project is to evaluate the efficacy of preoperative erector spinae blocks in arthroscopic hip surgery. This will be a prospective randomized controlled trial.
Detailed Description
The aim of this project is to evaluate the efficacy of preoperative erector spinae blocks in arthroscopic hip surgery. This will be a prospective randomized controlled trial. The control group will not receive a preoperative block prior to surgery, but will receive local anesthetic at the surgical site at the conclusion of the surgery. The study group will receive a preoperative block and local anesthetic. The primary outcomes will be pain levels and opioid consumption in the post-operative care unit. The secondary outcomes will be pain levels and opioid consumption post-operatively, and functional outcome measures.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All patients undergoing hip arthroscopy for femoroacetabular impingement
- •Ages 13-50
- •Individuals who have the capacity to provide consent or assent for themselves
Exclusion Criteria
- •Hip arthroscopy for any other reason (not undergoing labral repair, acetabuloplasty, and femoral osteochondroplasty)
- •Revision surgery
- •Known narcotic use in the 6 months prior to surgery
- •Workman's compensation patient
- •Pregnancy
Outcomes
Primary Outcomes
Post Anesthesia Care Unit Pain
Time Frame: 6 hours post-operatively
Visual analogue pain score at the time of discharge from the Post Anesthesia Care Unit in which 0 equals no pain and 10 equals extreme pain
Post Anesthesia Care Unit Opioids
Time Frame: 6 hours post-operatively
Total morphine milligram equivalents of administered in the post-operative care unit
Secondary Outcomes
- Hip disability and Osteoarthritis Outcome Score(1 year post-operatively)
- Patient Reported Outcomes measurement Information System Score(1 year post-operatively)
- Range Of Motion(1 year post-operatively)
- Outpatient Opioids(4 weeks post discharge)
- Outpatient Visual Analog Scale scores(4 weeks post discharge)