Efficacy and Safety of Low Dose Rivaroxaban in Patients With Anterior Myocardial Infarction

Sponsor
Sohag University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05744804
Collaborator
(none)
150
1
2
9
16.6

Study Details

Study Description

Brief Summary

Despite the use of guideline directed optimal medical therapy, 12% of patients with stable coronary heart disease and 18% of patients with recent acute coronary syndrome experience recurrent major adverse cardiovascular events 1. The risk of recurrent cardiovascular events may be related to persistent elevation of thrombin beyond the index event 2,3

which leads to progression of cardiovascular disease by inducing inflammation, endothelial dysfunction and thrombosis 4. In patients with coronary heart disease, vitamin K antagonists (VKAs) and direct oral anticoagulants (DOACs) have been explored as secondary prevention strategies and have shown cardiovascular benefits at the cost of higher bleeding events 5,6,7,8.

howeverLeft ventricular thrombus (LVT) usually appearswithin 1 month after ST-segment elevation myocardial infarction (STEMI) and mostlyforms after anterior STEMI.9,11Although the prevalenceof LVT after acute myocardial infarction hasdecreased dramatically in modern times due to the progress of reperfusion therapy, LVT incidence in patients with anterior STEMI remains at 4% to 26%.10,12 It complicates acute myocardial infarction and is associated with a higher incidence of poor outcomes.9

Condition or Disease Intervention/Treatment Phase
  • Drug: -group of patients(75 patients) will receive low dose rivaroxaban myocardial infarction plus (acetylsalicylic acid 75 mg and clopidogrel 75 mg
  • Drug: (acetylsalicylic acid 75 mg once daily orally and clopidogrel 75 mg once daily orally only)
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Efficacy and Safety of Low Dose Rivaroxaban in Patients With Anterior Myocardial Infarction
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: -group of patients(75 patients) will receive low dose rivaroxaban

-group of patients(75 patients) will receive low dose rivaroxaban (rivaroxaban 2.5 mg twice daily orally) for 1 month after anterior ST-segment myocardial infarction plus dual antiplatelet therapy (acetylsalicylic acid 75 mg once daily orally and cloppe

Drug: -group of patients(75 patients) will receive low dose rivaroxaban myocardial infarction plus (acetylsalicylic acid 75 mg and clopidogrel 75 mg
receive low dose rivaroxaban (rivaroxaban 2.5 mg twice daily orally) for 1 month after anterior ST-segment myocardial infarction plus dual antiplatelet therapy (acetylsalicylic acid 75 mg once daily orally and clopidogrel 75 mg once daily orally)

Active Comparator: control group of patients:

control group of patients: 75 Patients of anterior ST-segment myocardial infarction on dual antiplatelet therapy only

Drug: (acetylsalicylic acid 75 mg once daily orally and clopidogrel 75 mg once daily orally only)
control group of patients: 75 Patients of anterior ST-segment myocardial infarction on dual antiplatelet therapy only

Outcome Measures

Primary Outcome Measures

  1. Major adverse cardiovascular event [10 months]

    Major adverse cardiovascular event

  2. Left ventricular function [10 months]

    Left ventricular function

  3. Left ventricular thrombus [10 months]

    Left ventricular thrombus

  4. Transient Ischemic Attacks or cerebrovascular stroke [10 months]

    Transient Ischemic Attacks or cerebrovascular stroke

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients with anterior ST-segment myocardial infarction on acetylsalicylic acid and clopidogrel
Exclusion Criteria:
  1. Patients with liver cirrhosis.

  2. Patients with severe mitral stenosis .

  3. Patients with bleeding tendency (HASBLED score ≥ 3)

  4. Severe renal impairment ( creatinine clearance < 30 ml/min ).

  5. patients with prosthetic valve .

  6. patients on ticagrelor treatment

  7. patients with Atrial Fibrillation

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sohag University Hospital Sohag Egypt

Sponsors and Collaborators

  • Sohag University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Mohamed Elamir Saber, resident doctor at internal medecine department, Sohag University
ClinicalTrials.gov Identifier:
NCT05744804
Other Study ID Numbers:
  • soh-Med-23-01-09
First Posted:
Feb 27, 2023
Last Update Posted:
Feb 27, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 27, 2023