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Terminated Not applicable Interventional Results available

ATTUNE Cementless FB Tibial Base Clinical Study

ClinicalTrials.gov ID: NCT04630262

Public ClinicalTrials.gov record NCT04630262. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 3:06 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multi-Center Clinical Investigation of the ATTUNE® Cementless Fixed Bearing Tibial Base and Cementless Patella Implants in Total Knee Arthroplasty

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a prospective, multi-center, non-randomized, single arm observational study. The primary objective of this clinical investigation is to evaluate functional responder rates with an objective performance criteria (OPC) of 85% as measured by the KOOS questionnaire for the first 225 tibia (CR FB and PS FB combined) implanted with the ATTUNE Cementless FB tray (primary and revision procedures) and will be analyzed when these patients have passed the 1 year preferred post-op window.

Study identification

NCT ID
NCT04630262
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
DePuy Orthopaedics
Industry
Enrollment
80 participants

Conditions and interventions

Eligibility (public fields only)

Age range
22 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 8, 2022
Primary completion
Mar 30, 2023
Completion
Mar 30, 2023
Last update posted
Mar 3, 2025

2022 – 2023

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
Orthopaedic Specialty Institute Irvine California 92618
Coastal Orthopedics Bradenton Florida 34209
Florida Orthopaedic Associates DeLand Florida 32720
University of Florida Gainesville Florida 32611
American Hip Institute & Orthopedic Specialists Chicago Illinois 60018
Loyola University Medical Center Maywood Illinois 60153
Johns Hopkins Orthpaedic Surgery Baltimore Maryland 21044
Towson Orthopaedic Associates Baltimore Maryland 21204
Rubin Institute for Advanced Orthopedics Baltimore Maryland 21215
Orthopaedic Associates of Michigan Grand Rapids Michigan 49525
University of Missouri Columbia Missouri 65212
Mercy Clinic Springfield Ozark Missouri 65721
University Orthopaedic Associates, LLC Somerset New Jersey 08873
Orlin & Cohen Orthopedics Garden City New York 11530
Anderson Clinic Alexandria Virginia 22306

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04630262, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 3, 2025 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04630262 live on ClinicalTrials.gov.

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