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MAFT: METFORMIN FOR ATRIAL FIBRILLATION

Sponsor
Arab Contractors Medical Centre (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05878535
Collaborator
(none)
770
Enrollment
1
Location
2
Arms
22
Anticipated Duration (Months)
35
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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:

  • The Metformin Group (MG): will receive metformin oral tablets in addition to the standard rate/rhythm control strategy and anticoagulation.

  • The Placebo Control Group (PCG): will receive placebo oral tablets as a control group in addition to the standard rate/rhythm control strategy and anticoagulation.

Then both arms will be compared according to the these endpoints:

  • The primary endpoint is hospitalization due to an episodic AF or an AF with a rapid or slow ventricular response (in the case of permanent AF).

  • The secondary endpoint is a composite of non-fatal major cardiovascular adverse events or non-cancer death.

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.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed 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:

  • General and Local cardiac examination.

  • CBC.

  • Chemistry Panel including KFTs, LFTs.

  • Serum electrolytes levels.

  • Resting surface 12 leads ECG.

  • Baseline echocardiography.

  • Interventions:

  • Drug: metformin 850 mg oral tablets. Prescribed: Once daily PO with meals and 200 mL of water. The dose can be up-titrated to 1500-2000 mg divided q8-12hr with meals in enrolled diabetic patients as a monotherapy or combined with sulfonylurea.

Other Name: Glucophage.

  • Drug: Placebo oral tablets. Prescribed: Once daily PO with meals and 200 mL of water. Other Name: Placebo

  • Study Arms:

  • 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 primary endpoint is hospitalization due to an episodic AF or an AF with a rapid or slow ventricular response (in the case of permanent AF).

  • The secondary endpoint is a composite of non-fatal major cardiovascular adverse events or non-cancer death.

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
770 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Efficacy And Safety Of Metformin For The Treatment Of Atrial Fibrillation
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Jan 1, 2025
Anticipated Study Completion Date :
Apr 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: The Metformin Group (MG)

The group (n=385) will receive metformin oral tablets in addition to the standard rate/rhythm control strategy and anticoagulation. • Drug: metformin 850 mg oral tablets. Prescribed: Once daily PO with meals and 200 mL of water. The dose can be up-titrated to 1500-2000 mg divided q8-12hr with meals in enrolled diabetic patients as a monotherapy or combined with sulfonylurea. Other Name: Glucophage.

Drug: Metformin
Metformin 850 mg oral tablets. Prescribed: Once daily PO with meals and 200 mL of water. The dose can be up-titrated to 1500-2000 mg divided q8-12hr with meals in enrolled diabetic patients as a monotherapy or combined with sulfonylurea.
Other Names:
  • Glucophage, Glumetza, and Riomet.

    		•
    Placebo Comparator: The Placebo Control Group (PCG)

    The group (n=385) will receive placebo oral tablets in addition to the standard rate/rhythm control strategy and anticoagulation. • Drug: Placebo oral tablets. Prescribed: Once daily PO with meals and 200 mL of water. Other Name: Placebo

    Drug: Placebo
    Placebo oral tablets. Prescribed: Once daily PO with meals and 200 mL of water.

    Outcome Measures

    Primary Outcome Measures

    1. Primary Endpoint [12 months since randomization]

      The primary endpoint is hospitalization due to an episodic AF or an AF with a rapid or slow ventricular response (in the case of permanent AF).

    Secondary Outcome Measures

    1. Secondary Endpoint [12 months since randomization]

      The secondary endpoint is a composite of non-fatal major cardiovascular adverse events or non-cancer death. 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.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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:

    • 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.

    • Alcoholism.

    • Pregnancy.

    • Lactation.

    • Chronic muscle diseases.

    • Acute trauma or burns within 2 weeks.

    • History of allergy to the implemented drugs.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Arab Contractors Medical Centre Cairo Egypt

    Sponsors and Collaborators

    • Arab Contractors Medical Centre

    Investigators

    • Principal Investigator: Eslam Abbas, MBBCh, MSC, Arab Contractors Medical Centre, and Dar El Salam Cancer Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Eslam Abbas, MBChB, MSc, Principal Invstigator, Arab Contractors Medical Centre
    ClinicalTrials.gov Identifier:
    NCT05878535
    Other Study ID Numbers:
    • #18101829
    First Posted:
    May 26, 2023
    Last Update Posted:
    May 30, 2023
    Last Verified:
    May 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Eslam Abbas, MBChB, MSc, Principal Invstigator, Arab Contractors Medical Centre
    Atrial Fibrillation, metformin, MACE.
    Additional relevant MeSH terms:
    Atrial Fibrillation
    Metformin

    Study Results

    No Results Posted as of May 30, 2023