A Randomized, Single-blind, Single-center Study Measuring the Effects of Adductor Canal Block Combined With IPACK Infiltration Compared to Adductor Canal Block Alone on Post-operative Pain and Opioid Consumption in Patients Undergoing HTO/DFO/TTO
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY
A randomized, single-blind, single-center study measuring the effects of adductor canal block combined with IPACK infiltration compared to adductor canal block alone on post-operative pain and opioid consumption in patients undergoing high tibial osteotomy (HTO)/distal femoral osteotomy (DFO)/tibial tubercle osteotomy (TTO).
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:
• Patients between 18 and 75 years of age
• Patients undergoing HTO/DFO/TTO.
• American Society of Anesthesiologists (ASA) I or II
Locations
United States
New York
NYU Langone Health
RECRUITING
New York
Contact Information
Primary
Laith Jazrawi, MD
Laith.jazrawi@nyulangone.org
646-501-7223
Time Frame
Start Date: 2025-04-28
Estimated Completion Date: 2027-06-28
Participants
Target number of participants: 100
Treatments
Experimental: Adductor Canal Block (ACB) + IPACK Block
Participants receive ACB with IPACK block.
Active_comparator: Isolated Adductor Canal Block
Participants receive ACB only.
Related Therapeutic Areas
Sponsors
Leads: NYU Langone Health