Status:
RECRUITING
IPACK on Early Pain Scores After ACL Reconstruction
Lead Sponsor:
Loyola University
Conditions:
Pain, Postoperative
Anterior Cruciate Ligament Injuries
Eligibility:
All Genders
16+ years
Phase:
PHASE4
Brief Summary
The goal of this clinical trial is to learn whether using an anesthetic technique called IPACK block will control pain after ACL reconstruction surgery. The main questions it aims to answer are: * if...
Detailed Description
Eligible patients will be approached for voluntary study participation after they have made the decision to pursue an elective ACL reconstruction surgery with Dr. John Miller of Loyola University Depa...
Eligibility Criteria
Inclusion
- All patients presenting to Dr. John Miller with the Department of Orthopedic Surgery, Sports Medicine Division, at Loyola University Medical Center electing to undergo ACL reconstruction surgery.
- Patients 16 and over
- English speaking patients
- Patients who have the capacity to make their own medical decisions and consent to the study
Exclusion
- Previous surgery on the operative knee
- Previous knee infection
- Chronic opioid use
- Have a known allergy to local anesthetics
- Patient using autograft (cadaver) for ACL reconstruction.
Key Trial Info
Start Date :
August 3 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 3 2026
Estimated Enrollment :
78 Patients enrolled
Trial Details
Trial ID
NCT05985629
Start Date
August 3 2023
End Date
August 3 2026
Last Update
August 14 2023
Active Locations (1)
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1
Loyola University Medical Center
Maywood, Illinois, United States, 60153