Minimal invasive knee surgery; is it less traumatic? A pilot study

Completed

• Conditions: artrosis; total knee arthroplasty; 10023213

• Registration Number: NL-OMON30180
• Lead Sponsor: Maaslandziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 18 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 40

Inclusion Criteria

- patients receiving a primary total knee arthroplasty
- patients with osteoarthritis or avascular necrosis

Exclusion Criteria

- pregnancy
- clinical relevant disorders, like rheumatoid arthritis, previous knee surgery, standard use of anticoagulantia
- unwilling and unable to cooperate in the study

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Hemoglobin will be determined in terms of blood loss. Blood loss is also<br /><br>measured during the operation and post-operatively in terms of drainporduction.<br /><br>H-FABP tissue damage and IL-6 inflammation reactions<br /><br>Furthermore the patient will be standard evaluated in terms of range of motion,<br /><br>prothesis alignement and pain</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>None</p><br>