Status and phase
Conditions
Treatments
About
The aim of this multicenter, pragmatic, open-label, randomized, placebo-controlled clinical trial is to test whether repurposing metformin for the treatment of atrial fibrillation will be effective in decreasing patients' hospitalization, adverse major cardiovascular events, and non-cancer death.
Participants will be randomized into 2 study arms (385 participant each), whereby:
Then both arms will be compared according to the these endpoints:
The non-fatal major cardiovascular adverse events include:
Full description
Type of The Study: Interventional, Placebo-Controlled Clinical Trial.
Therapeutic Area: Cardiology, Arrhythmia.
Purpose: Treatment.
Aim: Whether repurposing metformin for the treatment of atrial fibrillation will be effective in decreasing patients' hospitalization, adverse major cardiovascular events, and non-cancer death.
Assignment: Parallel.
Allocation: Randomized.
Masking: Pragmatic, Open-Label.
Duration: 12 months of follow-up.
Rationale: Atrial fibrillation (AF) is the most common heart arrhythmia [1], in which atria contract rapidly and irregularly and the contraction of atria and ventricles is no longer coordinated. Current guidelines for the treatment of AF recommend medication to avoid blood clotting and stroke, control heart rate, and restore sinus rhythm. However, the available treatments show limited efficiency and may have side effects associated with increased morbidity and mortality [2], emphasizing an urgent need for new or repurposed therapies. Lal and colleagues [3] reported an integrative approach-combining transcriptomics, iPSCs, and epidemiological evidence-to identify and repurpose metformin, a main first-line medication for the treatment of type 2 diabetes, as an effective risk reducer for atrial fibrillation. Interestingly, metformin enhances the life span in invertebrate and vertebrate laboratory models [4], and similar gene-expression-based drug-repurposing studies targeting aging identified metformin, among others, as a pro-longevity agent [5]. Diabetes and AF are both age-associated and often co-morbid conditions. Metformin is being tested in the Targeting Aging with Metformin (TAME) trial [6] to develop effective next-generation drugs to increase healthspan and lifespan. Additionally, metformin seems to be associated with a lower risk of atrial fibrillation and ventricular arrhythmias as compared with another anti-diabetic drug category which is sulfonylureas [7]. The potential antiarrhythmic role of metformin in patients with AF could be due to the effects of metformin on preventing the structural and electrical remodeling of the left atrium via attenuating intracellular reactive oxygen species, activating 5' adenosine monophosphate-activated protein kinase, improving calcium homeostasis, attenuating inflammation, increasing connexin-43 gap junction expression, and restoring small conductance calcium-activated potassium channels current [8]. Despite the solid preclinical, integrative, and retrospective analyses, the effect of metformin on patients with AF regarding morbidity and mortality has not be established using a perspective, randomized, controlled trial.
Inclusion Criteria: Age more than 20 years and less than 65 years, willing and able to provide written informed consent prior to performing study procedures, and diagnosed by atrial fibrillation (first detected, paroxysmal, persistent, longstanding persistent, or permanent).
Exclusion Criteria: Critically-ill patients who are admitted to ICU, advanced congestive heart failure, liver cell failure, chronic kidney disease with eGFR <45 mL/min/1.73 m², diabetic ketoacidosis with or without coma, concomitant treatment with carbonic anhydrase inhibitors, septicemia, shock, hypoxia, dehydration, blood dyscrasias, pregnancy, lactation, chronic muscle diseases, acute trauma or burns within 2 weeks, and history of allergy to the implemented drugs.
Methods: 770 enrolled AF patients who are candidates for metformin treatment according to the study criteria at the time of presentation, will undergo the following at the time of enrollment and during the bimonthly follow-ups:
Interventions:
Other Name: Glucophage.
Drug: Placebo oral tablets. Prescribed: Once daily PO with meals and 200 mL of water. Other Name: Placebo
The Metformin Group (MG): 385 patients will receive metformin oral tablets in addition to the standard rate/rhythm control strategy and anticoagulation.
The Placebo Control Group (PCG): 385 patients will receive placebo oral tablets as a control group in addition to the standard rate/rhythm control strategy and anticoagulation.
Endpoints:
The non-fatal major cardiovascular adverse events include:
Hospitalization due to heart failure.
Non-fatal myocardial infarction.
Non-fatal stroke.
Hospitalization due to unstable angina.
• Safety: In terms of safety, a composite of metformin side effects comprising GIT symptoms, hypoglycemia, and lactic acidosis will be considered.
Ethics: The study will be conducted in compliance with human studies committees' regulations of the authors' institutions and COPE guidelines, including patient consent as appropriate.
Competing Interests: The authors will declare any commercial or financial relationships that could be construed as a potential conflict of interest.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Willing and able to provide written informed consent prior to performing study procedures.
Atrial fibrillation (first detected, paroxysmal, persistent, longstanding persistent, or permanent)*.
* Types of atrial fibrillation:
First detected: only one diagnosed episode.
Paroxysmal: recurrent episodes that stop on their own in less than seven days.
Persistent: recurrent episodes that last more than seven days.
Longstanding persistent: recurrent episodes that last more than twelve months.
Permanent: atrial fibrillation that has been accepted, and for which a solely rate control strategy has been decided upon.
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
770 participants in 2 patient groups, including a placebo group
Loading...
Central trial contact
Eslam Abbas, MBBCh, MSC
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal