Apixaban Prophylaxis for Prevention of Left Ventricular Thrombus Following Anterior Myocardial Infarction

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-75
SponsorNational Institute of Cardiovascular Diseases, Pakistan

About this trial

The objective of this randomized controlled trial is to compare the safety and efficacy of low dose Apixaban (2.5 mg bid) in addition to guideline directed medical therapy vs guideline directed medical therapy alone in the prevention of left ventricular thrombus formation (after 30-days) following primary PCI in patients with acute anterior myocardial infarction with severe LV dysfunction.

Eligibility criteria

Qualifiers

Patients aged 18-65 years

Presenting with acute anterior STEMI

Severe LV dysfunction (EF<35%) with antero-apical akinesis, dyskinesis, or aneurysm

WIHTOUT evidence of LV thrombus.

Disqualifiers

Patients with previous anterior myocardial infarction or LAD revascularization procedures

Patients with cardiogenic shock

Patients with LV thrombus

Patients with advanced CKD (Cr > 2 and those on hemodialysis)

Trial design

Treatments tested in this trial

  • Apixaban 2.5 MG PO BID
  • Control (Standard treatment)

Treatment groups

472 Participants
are divided into 2 treatment groups