Patient Blinded Randomized Clinical Trial comparing two types of mobile bearing unicondylar knee replacement

Recruiting

• Conditions: Arthroplasty, Knee

• Registration Number: NL-OMON29323
• Lead Sponsor: SCORE

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 236

Inclusion Criteria

1. Age > 18

2. BMI < 40

Exclusion Criteria

1. Co-morbidity influencing the outcome of the implant.

2. Hypersensetivity to metals.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The Oxford Knee Score.

Secondary Outcome Measures

Name	Time	Method
1. The EuroQOL five dimensions questionnaire (EQ-5D) <br /><br>2. Knee disability and Osteoarthritis Outcome Score-Physical Function Short Form<br /><br>3. A Numeric rating scale (NRS) for pain