Purpose

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.

Conditions

Eligibility

Eligible Ages
Between 10 Years and 35 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 10-35 years old - Recurrent patellar instability with at least one episode defined as either (1) a dislocated patella requiring reduction in the emergency department or (2) a convincing history for dislocation, associated with full giving way, and the following physical findings: (a) hemarthrosis or effusion, (b) tenderness along the medial retinaculum, and (c) apprehension when laterally directed force was applied to the patella or (3) MRI-documented dislocation with associated bone bruises

Exclusion Criteria

  • Previous ipsilateral knee surgery - Obligatory/fixed/habitual patella dislocation or subluxation - Unloadable inferior or lateral chondral damage on the patella that would require a tibial tubercle transfer for unloading purposes - Pathologic tibiofemoral instability

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Isolated MPFL Reconstruction Patients with recurrent patellar instability (2 or more dislocation and/or subluxation events) undergoing isolated MPFL reconstruction
  • Procedure: Medial Patellofemoral Ligament (MPFL) Reconstruction
    For 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.

Recruiting Locations

Stanford University
Redwood City, California 94063
Contact:
Monica Sri Vel
msvel@stanford.edu

University of Florida
Gainesville, Florida 32607
Contact:
Tyler LaMonica
lamontj@ortho.ufl.edu

Midwest Orthopaedics at Rush
Chicago, Illinois 60612

University of Iowa
Iowa City, Iowa 52242
Contact:
Shannon Ortiz
shannon-ortiz@uiowa.edu

Massachusetts General Hospital
Boston, Massachusetts 02114
Contact:
Serafina Zotter
szotter@mgh.harvard.edu

Boston Children's Hospital
Boston, Massachusetts 02115
Contact:
Emma Gossman
Emma.Gossman@childrens.harvard.edu

NYU Langone Health
New York, New York 10016
Contact:
Ivanka Bhambhani
Ivanka.Bhambhani@nyulangone.org

Hospital for Special Surgery
New York, New York 10021
Contact:
Simone Gruber
646-797-8947
grubers@hss.edu

Duke Health
Wake Forest, North Carolina 27587
Contact:
Courtney Pyles
courtney.pyles@duke.edu

Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio 45229
Contact:
Matthew Veerkamp
513-636-3775
Matthew.Veerkamp@cchmc.org

Ohio State University Wexler Medical Center
Dublin, Ohio 43016
Contact:
Michael Keller
Michael.Keller@osumc.edu

Oregon Health & Science University
Portland, Oregon 97239
Contact:
Albert Yim
yima@ohsu.edu

Scottish Rite for Children
Dallas, Texas 75219
Contact:
Bayley Selee
Bayley.Selee@tsrh.org

More Details

NCT ID
NCT06883396
Status
Recruiting
Sponsor
Hospital for Special Surgery, New York

Study Contact

Simone Gruber
646-797-8947
grubers@hss.edu

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.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.