the Dutch Stent Thrombosis Study
Completed
- Conditions
- in-stent thrombosisblood clot in previously implanted coronary stent10011082
- Registration Number
- NL-OMON39367
- Lead Sponsor
- Sint Antonius Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 4000
Inclusion Criteria
all patients suffering a stent thrombosis
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.
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) and follow-up<br /><br>characteristics</p><br>
- Secondary Outcome Measures
Name Time Method <p>Bleedings according to the TIMI criteria</p><br>