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The ATtune Knee Outcome Study

NCT04247672 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 900

Last updated 2022-04-27

No results posted yet for this study

Summary

To accomodate dissatisfied patients with a total knee arthroplasty (TKA) and improve outcomes, several knee systems have been developed. The cemented ATTUNE TKA shows superiority over other established knee systems at short-term, abating with longer follow-up. There have been no studies reporting on the results of the uncemented version of the ATTUNE. Therefore, the main objective of the current study was to report patient reported outcome measures (PROMs), survivorship and complications associated with the uncemented ATTUNE TKA.

Conditions

Interventions

DEVICE

Total Knee Arthroplasty (uncemented rotating platform ATTUNE)

All patients receive an uncemented ATTUNE rotating platform knee system.

Sponsors & Collaborators

  • Spaarne Gasthuis

    lead OTHER

Eligibility

Min Age
21 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-02-03
Primary Completion
2024-01-22
Completion
2036-01-22
FDA Device
Yes

Countries

  • Netherlands

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04247672 on ClinicalTrials.gov