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Scorpio NRG (eNeRGize) Cruciate Retaining (CR) Post-market International Outcome Study — Scorpio NRG  

Arthroplasty, Replacement, Knee Clinical Trial

Official title:
Scorpio NRG Prospective, Open-label, Post-market International Multicentre Outcome Study

Clinical Trial Summary

The purpose of this study is to collect basic function, radiographic and patient satisfaction data for observation and analysis.

Clinical Trial Description

Evaluation of the effect of the component design on functional performance by comparing postoperative Knee Society Scores (KSS) with preoperative. Evaluate post-operative radiographic findings. Evaluate the effect of component design on patient activity by comparing postoperative Lower Extremity Activity Scale (LEAS) with preoperative. Evaluate patient satisfaction using Short-Form-36 Health Survey (SF-36). Evaluate quality of life using Knee Injury and Osteoarthritis Outcome Score (KOOS) and EuroQuol-5 dimension patient questionaire (EQ-5D). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02524730
Study type Interventional
Source Stryker Orthopaedics
Contact
Status Completed
Phase N/A
Start date May 18, 2009
Completion date February 10, 2020
View Details
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