Prevention of Late Stent Thrombosis by an Interdisciplinary Global European effort
Recruiting
- Conditions
- in-stent thrombosisblood clot in previously implanted coronary stent10011082
- Registration Number
- NL-OMON47161
- Lead Sponsor
- Sint Antonius Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 3000
Inclusion Criteria
Cases: all patients suffering a stent thrombosis
Controls: patients without ST who underwent PCI with stent implantation on the same date (±5 days) of index PCI of matched case, in the same interventional centre and with the same indication will be enrolled.
Exclusion Criteria
Absence of an informed consent;If a case or matched control patient dies before written Informed Consent could be obtained the clinical data will be used for the study, but only if the researcher doesn*t have any suggestion that the patient would have declined his consent if he still would have been alive. The researcher will write 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, biochemical, angiographic, procedural, haematological,<br /><br>histopathological, genetic, visual (by means of OCT/IVUS) and follow-up<br /><br>characteristics. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Not applicable.</p><br>