A randomised clinical trial comparing minimal invasive (MIS) total knee replacement (TKR) with conventional total knee replacement

Completed

• Conditions: osteoarthrosis; worn out knee; 10005944

• Registration Number: NL-OMON35423
• Lead Sponsor: Reinier de Graaf Groep

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

osteoarthrosis

Exclusion Criteria

unwilling to participate

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main study parameters/endpoints: Outcome will be clinically measured using the<br /><br>Knee Society Score (KSS), Oxford knee score, SF-12, KOOS questionnaire, whilst<br /><br>radiographic outcomes will be evaluated through standard radiographic<br /><br>parameters. Discharge criteria will be checked at day 3 p.o.<br /><br><br /><br><br /><br>Amendement 1: Penetration dept and wide of bone cement</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Hb level day 3<br /><br>Walking stairs (one level)<br /><br>Transfers<br /><br>Pain VAS / medication<br /><br>cement penetration research</p><br>