Knee Functional Flexion Axis (FFA) data acquisition during Total Knee Arthroplasty with Stryker Knee Navigatio

Not Applicable

Completed

• Conditions: Osteoarthritis of the knee; Musculoskeletal - Osteoarthritis

• Registration Number: ACTRN12610000493044
• Lead Sponsor: Stryker Australia Pty Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2010-06-16
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Patients requiring unilateral or bilateral computer assisted knee arthroplasty.

Non-pregnant females.

Over 18 years of age at time of surgery.

Patients who understand the conditions of the study and are willing to participate.

Patients who are capable of, and have given, written informed consent to their participation in the study

Exclusion Criteria

Patients unable or unwilling to undergo a computerised
tomography scan.

Patients that suffer claustrophobia.

Patients less than 18 years of age at the time of surgery.

Study & Design

• Study Type: Interventional
• Study Design: Not specified