Acute Coronary Syndrome Clinical Trials

Find Acute Coronary Syndrome Clinical Trials Near You

Strategies for Antiplatelet Management Following Acute Coronary Syndrome

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This study is testing different blood-thinning treatment strategies for people who have had a heart attack and were successfully treated with a coronary stent procedure (PCI). All strategies tested are already approved for this condition and used inversally. This study will define which of the approved strategies is the best one. After PCI, patients usually receive two antiplatelet medicines for up to 12 months to help prevent another heart attack or stroke, but this treatment can also increase bleeding risk. This study will compare a shorter course of dual antiplatelet therapy followed by one antiplatelet medicine alone versus the standard 12-month course. In addition, the study will compare two commonly used antiplatelet drugs, prasugrel and ticagrelor. The goal is to find out which strategy best prevents death, heart attack, or stroke while minimizing serious bleeding. This study is not testing any new intervention, rather comparing approved drugs and approved durations of use.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• ≥18 years old

• Admitted because of an acute MI (either STEMI or NSTEMI).

• Invasive management during index admission with successful PCI.

• Able to consent.

Locations
Other Locations
Ireland
Mater Private Network Dublin
NOT_YET_RECRUITING
Dublin
Latvia
Paula Stradiņa klīniskā universitates slimnīca
NOT_YET_RECRUITING
Riga
Norway
Oslo University Hospital, Ullevål.
NOT_YET_RECRUITING
Oslo
Poland
Saint John Paul II Hospital in Cracow
NOT_YET_RECRUITING
Krakow
Spain
Fundación Jiménez Díaz University Hospital
RECRUITING
Madrid
Contact Information
Primary
Noemi Escalera, PT
noemi.escalera@cnic.es
+34 91 4531200 (ext 5401)
Backup
Lucia Llanos, MD PhD
lucia.llanos@quironsalud.es
Time Frame
Start Date: 2026-09-02
Estimated Completion Date: 2030-01
Participants
Target number of participants: 8100
Treatments
Active_comparator: Prasugrel 12 months DAPT
Prasugrel-based 12 months DAPT
Experimental: Prasugrel abbreviated DAPT
Prasugrel-Based DAPT for 1 to 3 Months, Followed by Prasugrel Monotherapy Through 12 Months After MI
Experimental: Ticagrelor 12 months DAPT
Ticagrelor-based 12 months DAPT
Experimental: Ticagrelor abbreviated DAPT
Ticagrelor-Based DAPT for 1 to 3 Months, Followed by Prasugrel Monotherapy Through 12 Months After MI
Sponsors
Collaborators: Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III
Leads: Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz

This content was sourced from clinicaltrials.gov

Similar Clinical Trials