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Evaluation of Post-Operative Recovery in ATTUNE® Total Knee Arthroplasty

NCT02339610 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2019-08-28

No results posted yet for this study

Summary

This post-marketing investigation will evaluate the rate of recovery of the ATTUNE knee from the time of surgery through the 6 month endpoint in patients with severely painful and/or severely disabling Non-inflammatory Degenerative Joint Disease (NIDJD).

Conditions

  • Non-inflammatory Degenerative Joint Disease

Interventions

DEVICE

ATTUNE Primary, Cemented Total Knee Replacement

Patients will undergo a primary total knee replacement using one of the four implant configurations of the ATTUNE knee ( CR FB, CR RP, PS FB, PS RP).

Sponsors & Collaborators

  • DePuy Orthopaedics

    lead INDUSTRY

Principal Investigators

  • Verdonna Huey, MS, BSN, CCRP · DePuy Orthopaedics

Eligibility

Min Age
22 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-01
Primary Completion
2019-06-28
Completion
2019-06-28

Countries

  • Netherlands

Study Locations

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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 NCT02339610 on ClinicalTrials.gov