Clinical Trials Directory

Trials / Completed

CompletedNCT03401450

Optimal Location of Nerve Block to Minimize Perioperative Opioid Administration in ACL Surgery: Comparing True Adductor Canal to Proximal Block

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
69 (actual)
Sponsor
NYU Langone Health · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

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

Conditions

Interventions

TypeNameDescription
DRUGACB within true AC with bupivacaine 0.5% 20ccThe adductor canal block (ACB) is more commonly being used to provide post-operative analgesia since it provides a sensory block with minimal motor block.
DRUGACB proximal to true AC with bupivacaine 0.5% 20ccPatients will receive ultra-sound guided single femoral triangle block injection with 20 mL of 0.5% bupivicaine

Timeline

Start date
2018-02-01
Primary completion
2019-01-25
Completion
2021-06-29
First posted
2018-01-17
Last updated
2023-07-14
Results posted
2020-12-23

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03401450. Inclusion in this directory is not an endorsement.