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Clinical Trial Summary

This is a prospective, randomized, single blinded trial involving human subjects. The goal of this study is to determine an optimal location (proximal or distal) for the nerve block and whether it will make a difference in how much opioid the patient will receive during and after surgery. Ultrasound will identify the adductor canal and the proximal end of the adductor canal/apex of the femoral triangle to determine the location of the blocks. Their will be two randomized groups: 1. ACB within true AC with bupivacaine 0.5% 20cc2. ACB proximal to true AC with bupivacaine 0.5% 20cc


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03401450
Study type Interventional
Source NYU Langone Health
Contact
Status Completed
Phase Phase 4
Start date February 1, 2018
Completion date June 29, 2021