iPACK for Post-op Pain Following ACL Reconstruction

Status Completed

Clinical Trial Summary

This study will consist of patients 12 years and older undergoing ACL reconstruction using a quadriceps or bone-patella tendon bone (BTB) graft. The patients will be randomized to adductor canal block alone, or adductor canal block + iPACK block. The primary goal will be to determine the differences in postoperative pain during the first 72 hours when comparing the two groups. Secondary outcomes will include opioid utilization during the first 72 hours postoperatively and range of motion including terminal knee extension at postoperative follow-up visits.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

ACL Injury
Anterior Cruciate Ligament Injuries
Pain, Postoperative
Post Operative Pain

Clinical Trial Details

NCT number	NCT05498870
Study type	Interventional
Source	Medical University of South Carolina
Contact
Status	Completed
Phase	Phase 4
Start date	July 27, 2022
Completion date	August 14, 2023

View Details

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