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Active, not recruiting Not applicable Interventional

14022 ATTUNE Cementless RP Clinical Performance Evaluation

ClinicalTrials.gov ID: NCT02839850

Public ClinicalTrials.gov record NCT02839850. 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 1, 2026, 5:48 PM 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 Evaluation of the ATTUNE Cementless Rotating Platform Total Knee Arthroplasty

Brief summary

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

The primary objective of this study is to examine the change from pre-operative baseline to two year postoperative functional performance improvement for the ATTUNE primary, cementless TKA RP system as measured with the KOOS questionnaire (KOOS-ADL sub-score). This will be carried out for two configurations: cruciate retaining rotating platform (ATTUNE Cementless CR RP) and posterior stabilized rotating platform (ATTUNE Cementless PS RP).

Study identification

NCT ID
NCT02839850
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
DePuy Orthopaedics
Industry
Enrollment
540 participants

Conditions and interventions

Conditions

Interventions

Device

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
Aug 31, 2016
Primary completion
Aug 31, 2027
Completion
Aug 31, 2027
Last update posted
Aug 27, 2026

2016 – 2027

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
Colorado Joint Replacement Denver Colorado 80210
Florida Research Associates DeLand Florida 32720
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756
New London Hospital New London New Hampshire 03257
Rothman Institute Egg Harbor New Jersey 08234
SUNY downstate Medical Center Brooklyn New York 11203
UNC Chapel Hill Chapel Hill North Carolina 27599
Associated Orthopaedics of Kingsport Kingsport Tennessee 37660
Texas Tech University Heath Science Center Lubbock Texas 49416
Hampton Roads Orthopaedics and Sports Medicine Newport News Virginia 23606

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02839850, 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 Aug 27, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02839850 live on ClinicalTrials.gov.

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