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Scorpio Posterior Stabilised (PS) vs Scorpio NRG ("Energize") PS - Total Knee Arthroplasty — ScorpioNRGPS  

Arthroplasty, Replacement, Knee Clinical Trial

Official title:
Scorpio PS vs Scorpio NRG PS - Total Knee Arthroplasty Comparative Investigation of Function

Clinical Trial Summary

Single-centre, prospective, randomized comparative study to compare the maximum flexion and Chair Raise achievement ratios of the Scorpio PS and and the Scorpio NRG PS. Documentation of all complications.

Clinical Trial Description

Surveillance design: Single-centre, prospective, randomized comparative study. Objectives: To compare the maximum flexion (active and passive) and Chair Raise achievement ratios. All complications will be documented. Number of subjects to be enrolled: All consecutive Scorpio patients are included until a group size of 88 is reached. Clinical evaluations: Chair raise test, Stair climb test, Western Ontario McMaster Osteoarthritis Index (WOMAC) patient self evaluation, EuroQuol - 5 dimension (EQ-5D) patient questionnaire. Standard clinical, functional and pain parameters (Knee Society Score), pre-operatively and post-operatively. All per- and post-op complications. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02520531
Study type Interventional
Source Stryker Orthopaedics
Contact
Status Completed
Phase N/A
Start date September 2010
Completion date June 28, 2018
View Details
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