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Prospective Post Approval Clinical Follow-Up Study of the Commercially Available U2 Knee™ System - "U-Propel Study"
NCT03060057 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate both short and long term clinical performance and safety of the commercially available U2 Knee™ System.
Conditions Studied
Interventions
- DEVICE U2 Knee™ System
Study Locations (4)
Florida
- Coastal Orthopedics — Bradenton
- Jacksonville Orthopaedic Institute — Jacksonville
- Orthopedic Center of Vero Beach — Vero Beach
Maryland
- Rubin Institute for Advanced Orthopedics — Baltimore
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2017-03-30 |
| Est. Completion | 2026-03-30 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03060057
The ClinicalTrials.gov registry entry for NCT03060057 describes a study currently listed as active not 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 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is United Orthopedic Corporation, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Osteo Arthritis Knee appearing as the primary indexed condition, and to 1 intervention — of which U2 Knee™ 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: NCT03060057 reports 4 study locations spanning 2 distinct geographic areas — top geographies include Florida, 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 NCT03060057 about?
NCT03060057 is a clinical study titled "Prospective Post Approval Clinical Follow-Up Study of the Commercially Available U2 Knee™ System - "U-Propel Study"". The purpose of this study is to evaluate both short and long term clinical performance and safety of the commercially available U2 Knee™ System.
What is the current status of trial NCT03060057?
This trial is currently active not recruiting. The enrollment target is 200 participants. The study started on 2017-03-30. Estimated completion is 2026-03-30.
What conditions does trial NCT03060057 study?
This clinical trial studies the following conditions: Osteo Arthritis Knee. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03060057?
The interventions under investigation include: U2 Knee™ System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03060057?
This trial is sponsored by United Orthopedic Corporation, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03060057 being conducted?
This trial has 4 study locations across Florida, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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