Condition: ST Elevated Myocardial Infarction · Dual Antiplatelet Therapy · Sponsor: Research Maatschap Cardiologen Rotterdam Zuid
The study is a multi-centre, Open-label, Randomized Controlled, 1:1 trial comparing Prasugrel-based short DAPT (30-45 days) followed by Prasugrel monotherapy versus standard DAPT regimen in STEMI patients in terms of safety and efficacy endpoints. In the subgroup of STEMI patients with MVD, a sub-randomization will allow a comparison between a complete revascularization OCT-guided versus complete revascularization angiography-guided stent in terms of efficacy and safety endpoints.
This description comes directly from the study's public registry record.
Valeria Paradies, MD · +31621620153 · paradiesV2@maasstadziekenhuis.nl
Ria van Vliet · +31644162844 · vlietM@maasstadziekenhuis.nl
Always discuss trial participation with your own doctor first.
| Imelda Bonheiden | Bonheiden, Belgium | Recruiting |
| AZ St.Jan | Bruges, Belgium | Recruiting |
| ZOL Genk | Genk, Belgium | Recruiting |
| UZ Leuven | Leuven, Belgium | Recruiting |
| AZ Delta | Roeselare, Belgium | Recruiting |
| FN BRNO | Brno, Czechia | Recruiting |
| Masaryk Hospital Usti nad Labem - | Hradec Králové, Czechia | Recruiting |
| Charles University Hospital | Prague, Czechia | Not Yet Recruiting |
| Asklepios Klinik Bad Oldesloe | Bad Oldesloe, Germany | Recruiting |
| Segeberger Kliniken | Bad Segeberg, Germany | Recruiting |
| University hospital Dresden | Dresden, Germany | Recruiting |
| Ospedale Papa Giovanni XXIII | Bergamo, Italy | Recruiting |
+ 15 more locations — full list on the registry record.
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT05491200