Validation of stent boosting versus intravascular ultrasound for assessing optimum deployment of coronary stents

Completed

• Conditions: Insufficient stent deployment; 10011082

• Registration Number: NL-OMON31367
• Lead Sponsor: Catharina-ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 24 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

Patients undergoing stent implantation.

Exclusion Criteria

Any unstable condition.
Small or toruous coronary arteries.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>Optimum stent deployment according to the established criteria as described in<br /><br>the appendix of the protocol. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Not applicable. </p><br>