Treatment Of Atrial Fibrillation In Preserved Cardiac Function Heart Failure

Launched by ELECTROPHYSIOLOGY RESEARCH FOUNDATION · Nov 8, 2019

Keywords

ClinConnect Summary

This clinical trial is investigating new treatment options for patients who have heart failure with preserved function (HFpEF) and also experience atrial fibrillation (AF), a common heart rhythm problem. The study will explore how effective rhythm control therapies, like catheter ablation and antiarrhythmic medications, can be in managing both conditions together. The researchers aim to see if combining these treatments with optimized heart failure therapies can improve patient outcomes. This trial is important because many existing treatments for AF have not been tested specifically in patients with HFpEF, which affects about 43% of these patients.

To be eligible for the trial, participants should be at least 50 years old and have symptoms of heart failure along with paroxysmal (intermittent) or persistent atrial fibrillation. They also need to be on heart failure medications for at least 30 days before joining the study. Participants will receive careful monitoring and treatment during the trial, and they will need to provide written consent to take part. This study is currently recruiting, and if you or a loved one meet the criteria, it could be a chance to access new treatment options while contributing to important medical research.

Gender

ALL

Eligibility criteria

• • Inclusion Criteria: Patient with symptomatic Heart Failure with preserved systolic cardiac function \& paroxysmal or persistent atrial fibrillation who meet the following criteria
• • 1. Subjects must be willing and able to give written informed consent
• • 2. Outpatients ≥ 50 years of age, male or post- menopausal female patients; premenopausal female patients who are on and will maintain continuous birth control therapy during the study.
• • 3. Subjects must have documented HFpEF \& paroxysmal or persistent AF and satisfy one of the following inclusion criteria a) Consecutive patients with AF, symptomatic heart failure requiring diuretic therapy for at least 30 days prior to study entry b) Hospitalization for HF and/or AF in the past 12 months prior to catheter ablation with documented NT-pro BNP \>200pg/ml for patients not in AF or \> 600 pg/ml for patients in AF on screening ECG or NYHA class 2, 3 or ambulatory class 4 heart failure documented NT-pro BNP \>300pg/ml for patients not in AF or \> 900 pg/ml for patients in AF on screening ECG c).Evidence of structural heart disease defined as by at least 1 of the following echocardiography findings (any local measurement made during the screening epoch or within the 6 months prior to screening visit): 1) LA enlargement defined by at least 1 of the following: LA width (diameter) \>3.8 cm or LA length \>5.0 cm or LA area \>20 cm2 or LA volume \>55 ml or LA volume index \>29 ml/m2 2) LVH defined by septal thickness or posterior wall thickness \>1.1 cm d).Left ventricular ejection fraction \> 45% using standard imaging techniques at enrollment for study or in prior 6 months e).ECG documented paroxysmal or persistent atrial fibrillation f).Patients are candidates for a clinically indicated catheter ablation procedure, and Rate or Rhythm control antiarrhythmic drug therapy
• • 4. Patients should be on one or more standard heart failure drug therapy (ies) for heart failure with preserved cardiac function for at least 30 days
• • 5. Written informed consent for the clinically indicated study procedures
• • 6. Patients must be candidates for long-term OAC therapy based on clinical practice guidelines for treatment of AF. Guidelines for GFR as established for DOACSs will be applicable to all subjects.
• Exclusion Criteria:
• • 1. Patients with HFpEF who were not on any drug therapy for HF or have uncontrolled hypertension defined as systolic BP \>180 mm Hg at screening or \>150 mm Hg on three or more antihypertensive drugs
• • 2. Patients with QRS duration of \>120 ms and intraventricular conduction defects who are or maybe candidates for or have received ventricular resynchronization therapy
• • 3. Recent (\<1 month) myocardial infarction or acute coronary syndrome
• • 4. Recent (\<3 months) coronary revascularization procedures
• • 5. Documented LA thrombus on TEE or any LVEF measurement \<40%
• • 6. Patients who are not candidates for Rate or Rhythm control drug therapy for AF
• • 7. Dilated cardiomyopathy due to potentially reversible cause e.g. myocarditis
• • 8. Contraindications to anticoagulant therapy or adverse event with prior Warfarin or DOAC therapy
• • 9. Creatinine clearance \<30ml/min or \>95ml/min
• • 10. Advanced hepatic disease, pulmonary disease clinically significant congenital heart disease, clinically significant pericardial constriction, hypertrophic cardiomyopathy, infiltrative cardiomyopathy, decompensated valvular heart disease likely to require surgical or percutaneous intervention during the trial
• • 11. Recent stroke (\<3 months) or thromboembolic event, transient ischemic attack or carotid angioplasty in the prior 3 months
• • 12. Recent (\<3 months) intracranial or other major bleeding event
• • 13. Candidates for heart or any other organ transplantation or left ventricular assist devices, recent (\< 3 months) valve or other cardiac surgery
• • 14. Patients requiring ACE inhibitor or ARB drug therapy for any reason
• • 15. History of hypersensitivity to antiarrhythmic drugs
• • 16. Patients with other clinically significant medical condition that precludes study participation
• • 17. Patients with life expectancy \< 1 year
• • 18. Premenopausal female patients, who are not on continuous birth control therapy or are likely to discontinue it at any time during the entire duration of study enrollment.
• • 19. Pregnant or nursing lactating mothers or women of childbearing potential who are not on effective contraceptive therapy
• • 20. Patients who have been noncompliant with medical regimens or have social or other issues precluding regular follow up, history of alcohol or drug abuse in past 12 months.