Cruciate Retaining vs Posterior Stabilised Total Knee Replacement: A Randomised Clinical Trial

Not Applicable

Recruiting

• Conditions: Osteoarthritis; Rheumatoid arthritis; Inflammatory and Immune System - Rheumatoid arthritis; Musculoskeletal - Osteoarthritis

• Registration Number: ACTRN12609000960257
• Lead Sponsor: Sir Charles Gairdner Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2009-11-06
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Primary total knee replacement

Exclusion Criteria

Patients will be excluded from the trial for tibial deformity (including past fracture or high tibial osteotomy) or valgus deformity.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Oxford Knee Score (OKS). This assesses knee function.[2 weeks, 6 weeks, 3 months, 12 months, 2 years, 5 years and 10 years post-operatively];Active Range of Motion in degrees measured with a goniometer[2 weeks, 6 weeks, 3 months, 12 months, 2 years, 5 years and 10 years post-operatively]

Secondary Outcome Measures

Name	Time	Method
6 minute walk test. This tests the distance a patient can walk in 6 minutes[2 weeks, 6 weeks, 3 months, 12 months, 2 years, 5 years and 10 years post-operatively]