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临床试验/NCT05878535
NCT05878535尚未招募2 期

The Efficacy And Safety Of Metformin For The Treatment Of Atrial Fibrillation

Arab Contractors Medical Centre1 个研究点 分布在 1 个国家目标入组 770 人开始时间: 2024年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
770
试验地点
1
主要终点
Primary Endpoint

研究概览

简要总结

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.

详细描述

  • 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

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.
  • Dehydration.
  • Blood Dyscrasias.
  • Alcoholism.
  • Pregnancy.
  • Lactation.
  • Chronic muscle diseases.
  • Acute trauma or burns within 2 weeks.
  • History of allergy to the implemented drugs.

研究组 & 干预措施

The Metformin Group (MG)

Active Comparator

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.

干预措施: Metformin (Drug)

The Placebo Control Group (PCG)

Placebo Comparator

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

干预措施: Placebo (Drug)

结局指标

主要结局

Primary Endpoint

时间窗: 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).

次要结局

  • Secondary Endpoint(12 months since randomization)

研究者

发起方
Arab Contractors Medical Centre
申办方类型
Other
责任方
Principal Investigator
主要研究者

Eslam Abbas, MBChB, MSc

Principal Invstigator

Arab Contractors Medical Centre

研究点 (1)

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