The National Dutch Stent Thrombosis Registry

Recruiting

• Conditions: in-stent thrombosis; blood clot in previously implanted coronary stent; 10011082

• Registration Number: NL-OMON47084
• Lead Sponsor: Sint Antonius Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 1000

Inclusion Criteria

Cases: all patients suffering a stent thrombosis.
Controls: patients without stent thrombosis who underwent PCI with stent implantation on the same date (± 14 days) of index PCI of matched cases, in the same interventional centre and with the same indication as the matched cases will be enrolled.

Exclusion Criteria

The absence of an informed consent (IC).
If a case patient dies before written IC could be obtained, the clinical data will be used for the study only if the researcher does not have any suggestion that the patient would have declined his consent if he would still be alive. The researcher will make a note in the CRF stating this assumption. The family will not be contacted and no blood samples will be stored.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>Clinical, angiographic, procedural, hematological, histopathological, genetic,<br /><br>visual (by means of OCT) en follow-up characteristics. </p><br>

Secondary Outcome Measures

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