The HF-AF ENERGY Trial: Attenuate atrial fibrillation with nicotinamide riboside (niagen)
Recruiting
- Conditions
- Atrial fibrillation10007521
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
• Patients diagnosed with paroxysmal or persistent AF
• Left ventricle function <=40%
• Implantable cardiac device (ICD) equipped with rhythm monitoring software
• Ischemic and/or non-ischemic cardiomyopathy
• Aged between 18-90 years
Exclusion Criteria
• Permanent AF
• Hemodynamic instability
• Absence of atrial sensing
• Malabsorption diseases
• Metabolic diseases
• Inflammatory disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Our primary objective is to investigate whether niagen normalizes blood-based<br /><br>energy metabolites, mitochondrial levels, and proteostasis levels. </p><br>
- Secondary Outcome Measures
Name Time Method <p>To examine whether niagen reduces AF burden in patients with ischemic and/or<br /><br>non-ischemic heart disease. </p><br>