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Platelet Function in Patients With an Acute Coronary Syndrome

Association Between the Antiplatelet Drug Efficacy/Safety and Platelet Function in Patients Treated With Novel Platelet Inhibitors Due to an Acute Coronary Syndrome

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01992484
Acronym
ATLANTIS-ACS
Enrollment
1000
Registered
2013-11-25
Start date
2012-08-31
Completion date
Unknown
Last updated
2013-11-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome (ACS)

Keywords

platelets, Acute coronary Syndrome (ACS), prasugrel, ticagrelor, aspirin

Brief summary

The aims of the study are to: * explore whether platelet reactivity in patients treated wih novel platelet inhibitors is associated with clinical outcome * investigate whether a therapeutic window exist for novel platelet inhibitors * investigate the incidence of adverse events under treatment with novel platelet inhibitors in the real life clinical scenario * investigate the association between genetic polymorphisms, inflammation, platelet reactivity and clinical outcome * investigate synergistic effects between aspirin and novel platelet inhibitors

Interventions

None listed

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Signed informed consent * Acute coronary syndrome at admission * Planned treatment with novel platelet inhibitors * Age \>18

Exclusion criteria

\* Participation in interventional trials

Design outcomes

Primary

MeasureTime frameDescription
Net clinical benefit.1 yearA composite of MACE and BARC=\>2 bleedings.

Secondary

MeasureTime frameDescription
MACE and Major bleeding1 yearMACE: the composite of stent thrombosis, cardiac death and myocardial infarction. Major Bleeding: BARC =\>2, TIMI major, GUSTO moderate-severe-life threatening.

Other

MeasureTime frame
single endpoints of acute coronary syndrome, myocardial infarction, cardiac death, all-cause death, urgent vessel revascularization (PCI or CABG), stroke.1 year

Countries

Austria

Contacts

Primary ContactJolanta M Siller-Matula, PD MD PhD
jolanta.siller-matula@meduniwien.ac.at0043 1 404004614

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026