Heart Failure Clinical Trial

The Use of Ranolazine for Atrial Fibrillation and Diastolic Heart Failure

Summary

The purpose of this study is to evaluate the efficacy of ranolazine in the prevention of recurrent atrial fibrillation in post-cardioversion patients with heart failure and preserved ejection fraction.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Male or non-pregnant female > 18 years of age;
Documentation of heart failure and who are in NYHA class II or III;
Documented history of symptomatic AF < 6 months in duration at the time of presentation, currently in AF at the time of the external electrical cardioversion, and successfully restored to normal sinus rhythm;
Percutaneous coronary intervention (PCI) patients who can be placed on anticoagulation with warfarin post-cardioversion (and not on rivaroxaban or dabigatran);
Demonstration of preserved ejection fraction (EF) by echocardiography;
Echocardiographic evidence of impaired diastolic filling.

Exclusion Criteria:

Known history of permanent or long-standing AF (> 6 months);
Other acutely reversible causes of AF, including but not limited to: hyperthyroidism, pericarditis, myocarditis or pulmonary embolism;
Known history of cirrhosis;
NYHA Class IV;
Myocardial Infarction, unstable angina, or coronary artery bypass graft surgery within three months prior to screening;
Percutaneous coronary intervention (PCI) within 4 weeks prior to screening, if these patients need to be placed on rivaroxaban or dabigatran post-cardioversion;
Clinically significant valvular disease;
Clinically significant pulmonary disease;
Stroke within 3 months prior to screening;
Creatinine clearance < 30 mL/min as calculated by Cockcroft-Gault formula;
Use of anti-arrhythmic drugs (Class Ia or IIIc) within 3 months prior to screening;
Concurrent use of drugs considered strong inhibitors of CYP3A;
Concurrent use of drugs considered as CYP3A inducers;
Prior treatment with ranolazine.

Study is for people with:

Heart Failure

Phase:

Phase 2

Estimated Enrollment:

8

Study ID:

NCT01887353

Recruitment Status:

Terminated

Sponsor:

Intermountain Health Care, Inc.

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There is 1 Location for this study

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Intermountain Medical Center
Murray Utah, 84107, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Phase:

Phase 2

Estimated Enrollment:

8

Study ID:

NCT01887353

Recruitment Status:

Terminated

Sponsor:


Intermountain Health Care, Inc.

How clear is this clinincal trial information?

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