Actively Recruiting
Adductor Canal Block and IPACK Block vs. Isolated Adductor Canal Block for Post-Operative Analgesia Following HTO/DFO/TTO
Led by NYU Langone Health · Updated on 2026-02-25
100
Participants Needed
1
Research Sites
113 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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).
CONDITIONS
Official Title
Adductor Canal Block and IPACK Block vs. Isolated Adductor Canal Block for Post-Operative Analgesia Following HTO/DFO/TTO
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients between 18 and 75 years of age
- Patients undergoing high tibial osteotomy (HTO), distal femoral osteotomy (DFO), or tibial tubercle osteotomy (TTO)
- American Society of Anesthesiologists (ASA) physical status I or II
You will not qualify if you...
- Patients younger than 18 or older than 75 years
- Patients with multi-ligament knee injury
- Patients undergoing concomitant cartilage procedure or anterior cruciate ligament reconstruction (ACLR)
- Patients with chronic pain using opioids for 3 months or longer
- Patients allergic to oxycodone
- Patients with diagnosed or self-reported cognitive dysfunction
- Patients with neurologic disorders affecting pain sensation
- Patients with history of drug or alcohol abuse
- Patients unable to understand or follow instructions
- Patients with severe liver disease, renal insufficiency, congestive heart failure, or significant heart disease
- Patients allergic or contraindicated to study medications or procedures
- Patients with body mass index (BMI) over 45
- Patients unable to comply with study procedures
- Pregnant patients (assessed by urine pregnancy test before surgery)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
NYU Langone Health
New York, New York, United States, 10016
Actively Recruiting
Research Team
L
Laith Jazrawi, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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