in-stent thrombosis
Conditions
Interventions
None listed
Sponsors
Sint Antonius Ziekenhuis
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: all patients suffering a stent thrombosis
Exclusion criteria
Exclusion criteria: Abcense 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) and follow-up characteristics | — |
Secondary
| Measure | Time frame |
|---|---|
| Bleedings according to the TIMI criteria | — |
Countries
Netherlands
Outcome results
None listed