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ACTIVE NOT RECRUITING NA

ATTUNE Revision System in the Revision Total Knee Arthroplasty Population

NCT03153475 · View on ClinicalTrials.gov ↗

Study Summary

Five-year, Prospective, multi-center, non-randomized, non-controlled study of the ATTUNE® Revision total knee prostheses, utilizing the fixed bearing (FB) and rotating platform (RP) tibial component with the posterior stabilizing (PS) femoral component in revision total knee arthroplasty.

Interventions

  • DEVICE ATTUNE Revision Knee System in Revision Total Knee Arthroplasty

Study Locations (20)

Other

  • The Gold Coast Centre for Bone and Joint Surgery — Gold Coast
  • St. John of God Murdoch Hospital — Perth
  • Krankenhaus der Barmherzigen Schwestern Linz Betriebsgesellschaft m.b.H. — Linz
  • MoRe Foundation — Antwerp

Colorado

  • Colorado Joint Replacement — Denver
  • Orthopaedic Center of the Rockies — Fort Collins

North Carolina

  • UNC Orthopaedics — Chapel Hill
  • OrthoCarolina Hip and Knee Center — Charlotte

Texas

  • Texas Institute for Hip & Knee Surgery — Austin
  • Fondren Orthopedic Group — Houston

California

  • Scripps Clinic Torrey Pines — San Diego

Connecticut

  • Orthopedic Partners — Niantic

Florida

  • Florida Orthopedic Associates — DeLand

Kentucky

  • Arthroplasty Foundation — Louisville

Trial Details

FieldValue
Enrollment Target 400 participants
Start Date 2017-05-30
Est. Completion 2029-03-31
Phase NA

Sponsor

DePuy Orthopaedics

43 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03153475

The ClinicalTrials.gov registry entry for NCT03153475 describes a study currently listed as active not 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 400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is DePuy Orthopaedics, which has 43 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 Revision Total Knee Arthroplasty appearing as the primary indexed condition, and to 1 intervention — of which ATTUNE Revision Knee System in Revision Total Knee Arthroplasty 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: NCT03153475 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Other, Colorado, North Carolina. 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 NCT03153475 about?

NCT03153475 is a clinical study titled "ATTUNE Revision System in the Revision Total Knee Arthroplasty Population". Five-year, Prospective, multi-center, non-randomized, non-controlled study of the ATTUNE® Revision total knee prostheses, utilizing the fixed bearing (FB) and rotating platform (RP) tibial component with the posterior stabilizing (PS) femoral component in revision total knee arthroplasty.

What is the current status of trial NCT03153475?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 400 participants. The study started on 2017-05-30. Estimated completion is 2029-03-31.

What conditions does trial NCT03153475 study?

This clinical trial studies the following conditions: Revision Total Knee Arthroplasty. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03153475?

The interventions under investigation include: ATTUNE Revision Knee System in Revision Total Knee Arthroplasty (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03153475?

This trial is sponsored by DePuy Orthopaedics, which has 43 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03153475 being conducted?

This trial has 20 study locations across California, Colorado, Connecticut, Florida, Kentucky. 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