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