NL-OMON55649CompletedNot Applicable
INDICO AF - Atrial Fibrillation in patients with an implantable cardioverter defibrillator and coronary artery disease. - INDICO AF
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Academisch Medisch Centrum
- Enrollment
- 50
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18 to 99 (—)
Inclusion Criteria
- •Age between 18 and 80 years
- •CAD, evident from a) previous myocardial infarction or b) revascularization
- •through PCI or CABG
- •LVEF<35%, quantified on MRI, with nuclear imaging or determined by
- •echocardiography
- •Willing and able to sign informed consent and to comply with the protocol and
- •with the follow-up
- •Life expectancy > 2 years
Exclusion Criteria
- •Unwilling to sign informed consent
- •Current atrial fibrillation
- •A history of atrial fibrillation not including postoperative atrial
- •fibrillation
- •Previous catheter or surgical ablation for atrial fibrillation
- •Current use or current indication of vitamin K antagonist or NOACs
- •Use of class 1 or 3 antiarrhythmic drugs for ventricular or supraventricular
- •arrhythmia ` other than AF
- •Prosthetic heart valves
- •Dilated or hypertrophic cardiomyopathy
- •Congenital heart disease for which surgical correction was performed
- •Inherited arrhythmia syndrome
- •Active malignant disease
- •Use of antracyclins in the history
- •Being pregnant or of child bearing potential
- •Life expectancy<2 years
Investigators
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