Patient specific MRI protocol enhancement and Post-operative (imaging-based) evaluation of patient specific Total Knee Arthroplasty

Withdrawn

• Conditions: cuttingblocks; Total knee arthroplasty; 10023213

• Registration Number: NL-OMON38682
• Lead Sponsor: niversitair Medisch Centrum Utrecht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Withdrawn
• Sex: Not specified
• Target Recruitment: 12

Inclusion Criteria

Men and women who are planned to undergo a total knee arthroplasty at UMC Utrecht

Exclusion Criteria

- Patients with previous total knee arthroplasty
- Patients with other prostheses or metal objects/hardware in the field of view (FOV) of the MRI knee coil
- Incapacitated persons
- All contra-indications for MR-imaging

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>- The main study parameter is scan failure-rate. Our goal is to reduce failure<br /><br>rate by minimizing the scan sensitivity for distortions and reduce scan time to<br /><br>prevent movement artefacts.<br /><br><br /><br>- Validation tool/protocol for placement goals in post-operative scans</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>N/A</p><br>