Reduction in contrast volume and radiation with Magnetic Navigation: a Prospective Randomised Trial

Completed

• Conditions: angioplasty; percutaneous coronary intervention; 10011082

• Registration Number: NL-OMON36899
• Lead Sponsor: Onze Lieve Vrouwe Gasthuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 300

Inclusion Criteria

§ Age>18 years
§ Elective presentation for PCI
§ Diagnostic coronary angiography films suitable for 3D reconstruction

Exclusion Criteria

Acute coronary syndromes (unstable angina, MI) and chronic total occlusions

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary endpoint is the total contrast used.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary endpoints will be<br /><br>1. the contrast needed to cross the lesion,<br /><br>2. the time needed to cross the lesion,<br /><br>3. the total procedural time,<br /><br>4. the total irradiation,<br /><br>5. angiographic success rates, and<br /><br>6. complications.</p><br>