Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Evaluate the Safety and Effectiveness of the Polymotion Hip Resurfacing (PHR) System Compared to Total Hip Arthroplasty

NCT06792539 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this clinical trial is to evaluate the safety and effectiveness of the Polymotion Hip Resurfacing (PHR) System compared to total hip arthroplasty, for adults who require hip resurfacing arthroplasty due to 1) non-inflammatory arthritis (degenerative joint disease) such as osteoarthritis, traumatic arthritis, or 2) mild dysplasia/developmental dislocation of the hip (DDH) up to Crowe Grade 1.

Interventions

  • DEVICE Polymotion Hip Resurfacing (PHR) System

Study Locations (10)

Florida

  • Florida Medical Clinic Orlando Health — Tampa

Illinois

  • Rush University Medical Center — Chicago

Maryland

  • Sinai Hospital / LifeBridge Health — Baltimore

New York

  • NYU Longone — New York

Ohio

  • Joint Implant Surgeons — New Albany

Oregon

  • Oregon Health & Science University — Portland

South Carolina

  • Midlands Orthopaedics & Neurosurgery — Columbia

Virginia

  • Hampton Road Orthopaedics — Newport News

Trial Details

FieldValue
Enrollment Target 238 participants
Start Date 2025-01-22
Est. Completion 2028-01
Phase NA

Sponsor

JointMedica

28 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06792539

The ClinicalTrials.gov registry entry for NCT06792539 describes a study currently listed as recruiting. It is categorized as NA, 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 238 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is JointMedica, which has 28 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Degenerative Joint Disease of Hip appearing as the primary indexed condition, and to 1 intervention — of which Polymotion Hip Resurfacing (PHR) System 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: NCT06792539 reports 10 study locations spanning 10 distinct geographic areas — top geographies include Florida, Illinois, Maryland. 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 NCT06792539 about?

NCT06792539 is a clinical study titled "Evaluate the Safety and Effectiveness of the Polymotion Hip Resurfacing (PHR) System Compared to Total Hip Arthroplasty". The goal of this clinical trial is to evaluate the safety and effectiveness of the Polymotion Hip Resurfacing (PHR) System compared to total hip arthroplasty, for adults who require hip resurfacing arthroplasty due to 1) non-inflammatory arthritis (degenerative joint disease) such as osteoarthritis,...

What is the current status of trial NCT06792539?

This trial is currently recruiting. It is a NA study. The enrollment target is 238 participants. The study started on 2025-01-22. Estimated completion is 2028-01.

What conditions does trial NCT06792539 study?

This clinical trial studies the following conditions: Degenerative Joint Disease of Hip, Dysplasia; Hip, Osteoarthritis of the Hip. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06792539?

The interventions under investigation include: Polymotion Hip Resurfacing (PHR) System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06792539?

This trial is sponsored by JointMedica, which has 28 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06792539 being conducted?

This trial has 10 study locations across Florida, Illinois, Maryland, New York, Ohio. 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