iPACK for Post-op Pain Following ACL Reconstruction

• Status: Recruiting
• Trial end date: 2025-01-01
• Target enrollment: 0
• Participant gender: All

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.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Medical University of South Carolina

Criteria

Inclusion Criteria:

• Age 12 years and older

• Patients who are scheduled to undergo an ACL reconstruction with quadriceps or BTB graft.

Exclusion Criteria:

• Any contraindication to receiving regional anesthesia. This may include infection at the site of injection, allergy to local anesthetic, or pre-existing nerve injury.

• Patients undergoing hamstring graft or allograft for ACL

• Pre-existing infection at the site of injury

• Patients on chronic opioid treatments

• Pre-existing sensory or motor deficit in operative extremity

• Patients having a revision of previous ACL reconstruction

• Pregnant and/or lactating women

• Weighs less than 40kg