Ticagrelor or Prasugrel Versus Clopidogrel in Elderly Patients With an Acute Coronary Syndrome and a High Bleeding Risk: Optimization of Antiplatelet Treatment in High-risk Elderly

Unstable Angina Clinical Trial

— POPular AGE  

Official title:

Ticagrelor or Prasugrel Versus Clopidogrel in Elderly Patients With an Acute Coronary Syndrome and a High Bleeding Risk: Optimization of Antiplatelet Treatment in High-risk Elderly

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02317198
• Other study ID #: PAACS01
• Status: Completed
• Phase: Phase 4
• Start date: June 2013
• Est. completion date: November 2019

Study information

• Verified date: May 2024
• Source: St. Antonius Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A randomized controlled, open label, multicenter trial with 1000 patients aged 70 years and older, presenting with Non-ST-elevation acute coronary syndrome. Patients will be randomized to either clopidogrel or the novel P2Y12 inhibitor (ticagrelor or prasugrel). Patients will be followed for one year for outcomes such as bleeding episode requiring medical intervention and net clinical benefit (all cause mortality, non-fatal myocardial infarction, non-fatal stroke, PLATO major and minor bleeding).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1011
• Est. completion date: November 2019
• Est. primary completion date: November 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 70 Years and older

Eligibility

Inclusion Criteria:

• At least 70 years of age.

• Hospitalization for NSTEMI or UA < 72 hours

Exclusion Criteria:

• Contraindication to P2Y12 inhibitors i.e. clopidogrel, prasugrel or ticagrelor:

• Unable or unwilling to give informed consent or have a life expectancy of less than one year.

• Having received thrombolytic therapy within the previous 24 hours.

• Severe renal function impairment needing dialysis.

• Confirmed or persistent severe hypertension (Systolic Blood Pressure (SBP) > 180 mmHg and/or Diastolic Blood Pressure (DBP) >110 mmHg) at randomization.

• At increased bleeding risk, at the investigator's opinion, e.g. because of malignancy.

• Cardiogenic shock (SBP = 80mmHg for >30 mins) or Intra-Aortic Balloon Pump (IABP) at the time of screening.

• History of major surgery, severe trauma, fracture or organ biopsy within 90 days prior to randomisation.

• Clinically significant out of range values for platelet count or haemoglobin at screening, in the investigator's opinion.

• ACS under dual antiplatelet therapy, e.g. aspirin with a P2Y12 inhibitor; clopidogrel, prasugrel, ticagrelor.

• Patients with a known CYP2C19 genotype at the time of randomization.

Related Conditions & MeSH terms

• Acute Coronary Syndrome
• Angina, Unstable
• Infarction
• Myocardial Infarction
• Non-ST Elevated Myocardial Infarction
• Non-ST-elevation Acute Coronary Syndrome
• Non-ST-elevation Myocardial Infarction
• Syndrome
• Unstable Angina

Intervention

Drug:
• Clopidogrel

• Ticagrelor or Prasugrel

Locations

Country	Name	City	State
Netherlands	St. Antonius hospital	Nieuwegein	Utrecht

Sponsors (10)

Lead Sponsor	Collaborator
St. Antonius Hospital	Gelderse Vallei Hospital, Gelre Hospitals, Isala, Leiden University Medical Center, Meander Medical Center, Medical Center Alkmaar, Medical Centre Leeuwarden, Rijnstate Hospital, UMC Utrecht

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	occurrence of any bleeding episode requiring medical intervention at 1 year after randomisation		One year
Primary	net clinical benefit at 1 year after randomisation	All cause mortality, non-fatal myocardial infarction, non-fatal stroke, PLATO major and minor bleeding	One year