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Evaluation of the Patellar LIFT System for Subjects With Patellofemoral Cartilage Degeneration

NCT06423300 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 245

Last updated 2025-12-11

No results posted yet for this study

Summary

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).

Conditions

  • Patellofemoral Osteoarthritis

Interventions

DEVICE

LIFT Implant

The LIFT implant provides a less invasive option for treatment of patellofemoral cartilage degeneration in the knee. the LIFT implant unloads the patellofemoral joint by elevating the patellar tendon to unload the joint compartment and realign the kneecap toward healthier cartilage

OTHER

Tibial Tubercle Osteotomy

Tibial Tubercle Osteotomy

Sponsors & Collaborators

  • ZKR Orthopedics Inc

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
22 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-19
Primary Completion
2027-09-30
Completion
2031-09-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06423300 on ClinicalTrials.gov