in-stent thrombosis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical, biochemical, angiographic, procedural, haematological, histopathological, genetic, visual (by means of OCT/IVUS) and follow-up characteristics. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not applicable. | — |
Countries
Netherlands