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RECRUITING

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

NCT06883396 · View on ClinicalTrials.gov ↗

Study 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.

Interventions

  • PROCEDURE Medial Patellofemoral Ligament (MPFL) Reconstruction

Study Locations (16)

New York

  • Mount Sinai — New York
  • NYU Langone Health — New York
  • Hospital for Special Surgery — New York

Ohio

  • Cincinnati Children's Hospital Medical Center — Cincinnati
  • Cleveland Clinic — Cleveland
  • Ohio State University Wexler Medical Center — Dublin

Massachusetts

  • Massachusetts General Hospital — Boston
  • Boston Children's Hospital — Boston

California

  • Stanford University — Redwood City

Florida

  • University of Florida — Gainesville

Illinois

  • Midwest Orthopaedics at Rush — Chicago

Iowa

  • University of Iowa — Iowa City

Minnesota

  • Mayo Clinic — Rochester

Trial Details

FieldValue
Enrollment Target 850 participants
Start Date 2023-01-01
Est. Completion 2027-12

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06883396

The ClinicalTrials.gov registry entry for NCT06883396 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 850 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hospital for Special Surgery, New York, which has 141 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 6 conditions, with Patellar Dislocation appearing as the primary indexed condition, and to 1 intervention — of which Medial Patellofemoral Ligament (MPFL) Reconstruction is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06883396 reports 16 study locations spanning 11 distinct geographic areas — top geographies include New York, Ohio, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06883396 about?

NCT06883396 is a clinical study titled "JUPITER 4.0 - Risk Factors for Failure of Isolated Medial Patellofemoral Ligament Reconstruction". 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 recons...

What is the current status of trial NCT06883396?

This trial is currently recruiting. The enrollment target is 850 participants. The study started on 2023-01-01. Estimated completion is 2027-12.

What conditions does trial NCT06883396 study?

This clinical trial studies the following conditions: Patellar Dislocation, Patellar Dislocation, Recurrent, Patellar Instability, Patellofemoral Dislocation, Patellofemoral Joint Dislocation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06883396?

The interventions under investigation include: Medial Patellofemoral Ligament (MPFL) Reconstruction (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06883396?

This trial is sponsored by Hospital for Special Surgery, New York, which has 141 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06883396 being conducted?

This trial has 16 study locations across California, Florida, Illinois, Iowa, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial