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Clinical Trials/ACTRN12618001858280
ACTRN12618001858280
Terminated
Phase 4

Randomized Evaluation of Beta Blocker and Angiotensin Converting Enzyme Inhibitor (ACEI) /Angiotensin Receptor Blocker (ARB) Treatment in MINOCA Patients.

The University of Adelaide0 sites71 target enrollmentNovember 15, 2018

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Myocardial Infarction With Non-obstructive Coronary Arteries
Sponsor
The University of Adelaide
Enrollment
71
Status
Terminated
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 15, 2018
End Date
May 31, 2023
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Age equal or greater than 18 years.
  • 2\. A clinical diagnosis of MINOCA, including:
  • a. Acute myocardial infarction – as per the universal myocardial infarction Criteria (Thygesen et al, 2018\)
  • b. Non\-obstructive coronary arteries – no lesion equal or greater than 50% in the potential infarct\-related artery.
  • c. No overt non\-ischaemic cause for the acute clinical presentation.
  • 3\. Left ventricle ejection fraction equal or less than 40% \- assessed by echocardiography, MRI or left ventriculography prior to
  • randomisation.
  • 4\. Written informed consent obtained

Exclusion Criteria

  • Any condition that may influence the patient's ability to comply with study protocol.
  • 2\. Pregnancy
  • 3\. Previous revascularization (CABG or PCI)
  • 4\. Myocarditis Diagnosis (Cardiac MRI proved myocarditis or a strong clinical suspicion
  • of myocarditis as a cause of the index event)
  • 5\. Clinical signs of heart failure
  • 6\. Contraindications for ACEI and ARB
  • 7\. Contraindications for beta\-blockers
  • 8\. Prior use of ACE\-I, ARB, or beta blockers, which must continue as per treating
  • 9\. New indication for beta\-blockers or ACEI/ARB other than as secondary prevention as

Outcomes

Primary Outcomes

Not specified

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