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Femoral Nerve Block Versus. Adductor Canal Nerve Block for Peri-Operative Analgesia Following Anterior Cruciate Ligament Reconstruction: Evaluation of Post-Operative Pain and Strength
All patients over the age of 16 undergoing primary or revision anterior cruciate ligament reconstruction with the use of bone-patellar-bone autograft are eligible for the study. Patients will be randomized pre-operatively to receive either an adductor canal nerve block (single injection) or a femoral nerve block (single injection). Post-operatively, the primary outcome measures of pain level using visual analog scale as well as narcotic and non-narcotic analgesic requirements will be measured.
Details
| Lead sponsor | Henry Ford Health System |
|---|---|
| Phase | NA |
| Status | COMPLETED |
| Enrolment | 78 |
| Start date | 2016-05 |
| Completion | 2017-12-31 |
Conditions
- Pain
Interventions
- Marcaine 0.25 % Injectable Solution
- Marcaine 0.25 % Injectable Solution
Primary outcomes
- Visual Analog Scale — Post-op Day 0-5
Every 4 hours the patient will record in their study binder their pain level on a scale from 1-10. They are instructed that a 1 signifies minimal pain that is nearly unnoticeable whereas a pain scale of 10 is the most intolerable pain imaginable. - Narcotic Requirement — Post-op Day 0-5
Every time a the prescribed narcotic is consumed, in this study it is Norco 5-325 (Hydrocodone-Acetaminophen), the subject is instructed to log their quantity consumed as well as the time consumed in the study binder provided to them
Countries
United States