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PS150 Total Knee Arthroplasty Outcomes Registry

NCT02319291 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 175

Last updated 2023-02-22

No results posted yet for this study

Summary

This registry is intended to evaluate the clinical outcomes of the DePuy P.F.C. Sigma PS150 RP Total Knee System. 200 participants will be enrolled prospectively or retrospectively and the follow up period will be 5 years. Data collection will include Radiographic Analysis, Knee Society Evaluation and Adverse Events.

Conditions

Interventions

DEVICE

P.F.C. Sigma PS150 RP Total Knee System

Total Knee Arthroplasty - surgical procedure to replace knee with metal implant

Sponsors & Collaborators

  • DePuy Orthopaedics

    lead INDUSTRY

Principal Investigators

  • Mark Dekkers, MBBS · Greenslopes Private Hospital, Brisbane

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-02-01
Primary Completion
2021-11-03
Completion
2021-11-03

Countries

  • Australia
  • South Korea

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 NCT02319291 on ClinicalTrials.gov