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Clinical Trials/NCT04625946
NCT04625946
Completed
Phase 4

Metformin as an Adjunctive Therapy to Catheter Ablation in Atrial Fibrillation

University of Michigan1 site in 1 country117 target enrollmentJanuary 19, 2021

Overview

Phase
Phase 4
Intervention
Metformin
Conditions
Atrial Fibrillation
Sponsor
University of Michigan
Enrollment
117
Locations
1
Primary Endpoint
Freedom from recurrent atrial arrhythmias by 12 months after a single ablation to eliminate AF
Status
Completed
Last Updated
7 months ago

Overview

Brief Summary

This clinical trial is being done to determine if metformin, a drug which is normally used in diabetes, can reduce atrial fibrillation in patients who are having an ablation for atrial fibrillation (AF). Atrial fibrillation is an abnormal heart rhythm which research has shown is related in part to obesity and diabetes.

It is anticipated that the participants treated in the metformin arm will have greater freedom from recurrent atrial arrhythmias after ablation.

Eligible participants enrolled in the trial will be assigned to one of the treatment arms (no treatment or metformin) and have follow-up visits up to approximately 1 year after the ablation. Additionally, all patients will also receive education on lifestyle changes and exercise which are standard of care.

Registry
clinicaltrials.gov
Start Date
January 19, 2021
End Date
August 10, 2025
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hakan Oral

Professor of Internal Medicine

University of Michigan

Eligibility Criteria

Inclusion Criteria

  • Body Mass Index (BMI) \>25 kilograms / square meter (kg/m2) with plan for rhythm control of atrial fibrillation by catheter ablation
  • All subjects must be able to understand and willing to sign a written informed consent document.

Exclusion Criteria

  • Individuals who are already taking metformin or other antidiabetic medications, including insulin
  • Known diabetes
  • Known allergy or Food and Drug Administration (FDA)-labeled contraindication to taking metformin (estimated glomerular filtration rate (eGFR)\<30 millilitres per minute (mL/min)/1.73 square meters (m2), hypersensitivity to metformin, acute or chronic metabolic acidosis)
  • Patients taking carbonic anhydrase inhibitors
  • eGFR below 30 mL/min per 1.73 m2 or other clinical diagnosis of advanced renal disease
  • Acute or chronic metabolic acidosis (serum bicarbonate \<22 milliequivalents per liter (mEq/L))
  • History of significant alcohol use (\>2 drinks/day on average)
  • History of hepatic dysfunction (serum bilirubin 1.5 times greater than ULN)
  • History of New York Heart Association (NYHA) Class III or IV heart failure
  • Pregnancy or nursing

Arms & Interventions

Metformin

Standard of care ablation with recommendations for lifestyle modification and metformin.

Intervention: Metformin

Metformin

Standard of care ablation with recommendations for lifestyle modification and metformin.

Intervention: Recommendations for lifestyle modification.

Metformin

Standard of care ablation with recommendations for lifestyle modification and metformin.

Intervention: AliveCor

Standard of care

Standard of care ablation with recommendations for lifestyle modification.

Intervention: Recommendations for lifestyle modification.

Standard of care

Standard of care ablation with recommendations for lifestyle modification.

Intervention: AliveCor

Outcomes

Primary Outcomes

Freedom from recurrent atrial arrhythmias by 12 months after a single ablation to eliminate AF

Time Frame: 12 months after ablation

There will be a 3 month blanking period after ablation during which recurrent atrial arrhythmias will not contribute to the primary endpoint.

Secondary Outcomes

  • Time to recurrence of atrial fibrillation after a 3 month blanking period of ablation(up to 1 year after after ablation)
  • Freedom from recurrent atrial arrhythmias at 1 year after ablation after the blanking period of 3 months(6 months after ablation)
  • Percent change in weight at 6 months after ablation(6 months after ablation)
  • Percent change in hemoglobin A1c at 6 months after ablation(6 months after ablation)
  • Freedom from recurrent atrial arrhythmias at 6 months after repeat ablation(6 months after a repeated ablation)
  • Atrial Fibrillation Severity Score (AFSS)(up to 12 months after ablation)
  • Percent change in weight at 3 months after ablation(3 months after ablation)
  • Percent change in hemoglobin A1C at 12 months after ablation(12 months after ablation)
  • Incidence of major procedural complications(up to 30 days)
  • Atrial Fibrillation related morbidity during follow-up(up to approximately 1 year after ablation)
  • Burden of Atrial Fibrillation assessed by AliveCOR Kardia Devices(3 months after ablation)

Study Sites (1)

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