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DSJ-2016-07 ATTUNE® Cementless CR RP Japan

NCT03193034 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 81

Last updated 2021-09-29

No results posted yet for this study

Summary

The primary objective is to investigate 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) in the Japanese patient population.

Conditions

Interventions

DEVICE

Cementless Total Knee Arthroplasty

Patients will undergo a primary total knee replacement using the configuration of the ATTUNE Cementless knee (CR RP)

Sponsors & Collaborators

  • Johnson & Johnson K.K. Medical Company

    collaborator INDUSTRY

  • DePuy Orthopaedics

    lead INDUSTRY

Principal Investigators

  • Kirstin Cosgrove · Sponsor GmbH

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2017-06-30
Primary Completion
2020-12-22
Completion
2021-06-30

Countries

  • Japan

Study Locations

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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 NCT03193034 on ClinicalTrials.gov