Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06883396

JUPITER 4.0 - Risk Factors for Failure of Isolated Medial Patellofemoral Ligament Reconstruction

Status
Recruiting
Phase
Study type
Observational
Enrollment
850 (estimated)
Sponsor
Hospital for Special Surgery, New York · Academic / Other
Sex
All
Age
10 Years – 35 Years
Healthy volunteers
Not accepted

Summary

The goal of this observational study is to learn about the outcomes of medial patellofemoral ligament (MPFL) reconstruction for the treatment of recurrent patellar instability. The main questions it aims to answer are: * What are the risk factors for recurrent patellar instability after MPFL reconstruction? * What functional outcomes do patients report after MPFL reconstruction? Participants undergoing MPFL reconstruction will answer survey questions about their knee and activity level 1 year and 2 years after surgery.

Detailed description

The JUPITER group consists of high-volume patellofemoral surgeons across the United States, and was organized to facilitate the collection of clinical and radiographic outcomes following surgical and non-surgical treatment of patellar instability. With this study (JUPITER 4.0), the group aims to prospectively enroll a new cohort of consecutive patients with recurrent patellar instability that would undergo isolated MPFL reconstruction regardless of radiographic measurements or anatomic risk factors to address two specific aims - 1) what patient, injury, and surgical factors lead to recurrent instability following isolated MPFL reconstruction and 2) the creation of an instability severity index score, with the long-term objective of identifying preoperatively, patients with a high risk of failure of an isolated MPFL reconstruction who may be better served with concomitant bony procedure.

Conditions

Interventions

TypeNameDescription
PROCEDUREMedial Patellofemoral Ligament (MPFL) ReconstructionFor the purposes of this study, isolated MPFL reconstruction is defined as MPFL reconstruction with a tendon graft, with or without additional soft tissue procedure(s) including lateral retinacular lengthening or release, patellofemoral chondroplasty and/or cartilage restoration. No patient in the study will receive a bony realignment procedure to treat patellar instability.

Timeline

Start date
2023-01-01
Primary completion
2026-12-01
Completion
2027-12-01
First posted
2025-03-19
Last updated
2026-02-13

Locations

16 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT06883396. Inclusion in this directory is not an endorsement.