New York, NYNCT06423300Now EnrollingIRB Ready

Patellofemoral Osteoarthritis Clinical Trial in New York, NY

Access cutting-edge patellofemoral osteoarthritis treatment through this clinical trial at a research site in New York. Study-provided care at no cost to qualified participants.

Sponsored by ZKR Orthopedics Inc

Quick Self-Assessment

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Expert Care in New York

Access patellofemoral osteoarthritis specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related patellofemoral osteoarthritis treatment provided free

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Check if you qualify for this patellofemoral osteoarthritis clinical trial in New York, NY

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Why Participate?

  • No-Cost Study Care

  • Local to New York

    Convenient for NY residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit New York site if eligible
  4. 4Begin participation

About This Patellofemoral Osteoarthritis Study in New York

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).

Sponsor: ZKR Orthopedics Inc

Who Can Participate

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

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in New York?

Yes, this clinical trial (NCT06423300) has an active research site in New York, NY that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Patellofemoral Osteoarthritis Treatment Options in New York, NY

If you're searching for patellofemoral osteoarthritis treatment options in New York, NY, this clinical trial (NCT06423300) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our New York research site is actively enrolling participants for this clinical trial. You'll receive care from experienced patellofemoral osteoarthritis specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all patellofemoral osteoarthritis clinical trials near you to find additional studies recruiting in your area.

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