Status:
COMPLETED
ACL Repair and Multimodal Analgesia
Lead Sponsor:
University of Wisconsin, Madison
Conditions:
Pain
Eligibility:
All Genders
18-55 years
Phase:
PHASE4
Brief Summary
This study will evaluate the effectiveness of an aggressive multimodal regimen versus standard multimodal for Anterior Cruciate Ligament (ACL) repair using hamstring graft for patients having surgery ...
Eligibility Criteria
Inclusion
- Patients of orthopedic surgeons on the study team scheduled for ACL repair using hamstring graft from the same leg will be considered for inclusion in this study. Other inclusion criteria are as follows:
- American Society of Anesthesiologists (ASA) physical status 1-3
- BMI of \< 40 kg/m2
- Consents to general anesthesia and pre-operative femoral nerve block for case
Exclusion
- Any contraindication to a femoral nerve block
- Allergy to local anesthetics, nonsteroidal anti-inflammatory medications, ketamine, acetaminophen, hydromorphone, oxycodone
- Peripheral or central nervous system disease
- Renal or hepatic impairment
- History of opioid dependence or current regular narcotic use
- Significant psychiatric disease
- Pregnancy or lactation (by verbal report)
- Seizure Disorder
- History of post-operative nausea and vomiting
- Latex allergy
- Clinically significant cardiac or pulmonary disease
Key Trial Info
Start Date :
April 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2017
Estimated Enrollment :
112 Patients enrolled
Trial Details
Trial ID
NCT01868425
Start Date
April 1 2013
End Date
December 1 2017
Last Update
March 30 2020
Active Locations (1)
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1
University of Wisconsin
Madison, Wisconsin, United States, 53705