Evaluation of the Patellar LIFT System for Subjects With Patellofemoral Cartilage Degeneration
Recruiting · NCT06423300 · Interventional (participants receive a specific treatment) · Lead sponsor: ZKR Orthopedics Inc
View the official record on ClinicalTrials.gov →Interventions studied
LIFT ImplantTibial Tubercle Osteotomy
What this trial is about
The PELICAN study is a prospective, non randomized, dual arm, multi-center clinical study comparing clinical outcomes of subjects treated with the LIFT Implant System to subjects treated with Tibial Tubercle Osteotomy (TTO).
Who can take part
Age range
22 Years to 65 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Patients age 22 to 65 years at time of screening
- Anterior knee pain due to patellofemoral cartilage degeneration (PCD) with an Modified Outerbridge score of ≥3 as assessed by an MRI on the study knee
- Body Mass Index (BMI) of ≤ 35
- Weight \< 300 lbs
- Anterior Knee Pain Score (AKPS) of ≤ 70 (0-100 scale)
- Visual Analog Score (VAS) of ≥ 40 (0-100 scale)
- Failure of at least 6 months of non-surgical treatment defined as at least one of the treatments (e.g. rest, bracing, physical therapy, targeted exercise, use of NSAIDs, activity level reduction or Confidential ZKR Orthopedics, CIP 0001 Page 11 of 55 Protocol Version: 1.0, 04JAN2024 modification, etc.) per AAOS Treatment of Osteoarthritis of the Knee; Evidence based guideline 3rd Edition 2021
Exclusion criteria
- PCD with an Modified Outerbridge Score of 2 or less at the study knee
- Clinical symptoms of the contralateral knee that preclude activities of daily living, stair climbing, stair descending, or require the use of an assist device
- History of patella dislocation or instability
- Patella alta or patella baja
- Known TT-TG distance \>20mm
- Patients requiring simultaneous cartilage grafting procedure, cartilage transplantation, or bone marrow stimulation
- Previous repair of a torn patellar tendon
- Prior TTO procedure or knee joint replacement (total or partial) of the study knee
- Joint modifying surgery (e.g., ligament reconstruction, meniscus repair, cartilage transplantation, microfracture, etc.) in the study knee within 6 months prior to planned index procedure date
- Arthroscopic surgeries in the study knee for joint lavage, meniscectomy, chondral debridement, and loose body removal within 3 months prior to planned index procedure
- Active infection, sepsis, osteomyelitis or history of septic arthritis in any joint
- Rheumatoid arthritis, other forms of inflammatory joint disease or autoimmune disorder
- History of avascular necrosis of any bone
- History of symptomatic patellar tendonitis of intrasubstance tear
- Insufficiency of the cruciate, collateral ligaments, or tendon which would preclude stability of the LIFT System
- Pathologic ligamentous injury (Lachman \> 1) or meniscus tearing
- Clinical symptoms of the femoral-tibial joint of the study knee that preclude activities of daily living, stair climbing, stair descending, or requires the use of an assist device
- Evidence (MRI, arthroscopy, etc.) of Modified Outerbridge Grade 4 degenerative arthritis in the femoral-tibial joint of the study knee that potentially explains patient symptoms
Where it is running
5 locations listed across 4 US states.
- Horizon Clinical Research - La Mesa, California, United States
- Hospital for Special Surgery - New York, New York, United States
- NYU Langone Health - New York, New York, United States
- Ohio State University - Jameson Crane Sports Medicine Institute - Columbus, Ohio, United States
- Oregon Health and Science University - Portland, Oregon, United States