Cardiac Contractility Modulation in Patients With Chronic Heart Failure and the Various Forms of Atrial Fibrillation
Heart Failure, Atrial Fibrillation, Left Ventricular Ejection Fraction
About this trial
This is an interventional treatment trial for Heart Failure focused on measuring Cardiac contractility modulation, Atrial Fibrillation, Heart Failure, Narrow QRS Complex, left ventricular ejection fraction
Eligibility Criteria
Inclusion Criteria:
- Documented HFrEF (20-40%)
- NYHA FC II-III for at least 3 months before screening
- AF
- Optimal CHF therapy and the absence of decompensations in ≥ 1 month.
Exclusion Criteria:
- Refusal to participate in the study
- Placement on the heart transplant waiting list, or post heart transplantation
- Terminal CHF
- Co-morbid diseases that may adversely affect the safety and / or efficacy of treatment
- Recent surgical intervention or trauma
- Medical conditions that limit life expectancy to 1 year.
Sites / Locations
- Alfiya Safiullina
Arms of the Study
Arm 1
Arm 2
Active Comparator
No Intervention
Optimizer device
Without Optimizer device
100 patients were enrolled sequentially, 100 patients were implanted with an optimizer smart against the background of optimal drug therapy for heart failure 100 patients were implanted with a CCM Optimizer device without an atrial lead, per the protocol specifications recived optimal drug therapy CHF The following studies were performed in the 100 patients with CHF and AF before implantation of the MCC device and after 2 and 6 и 12 months of follow-up: 12-channel ECG with an estimate of the width of the QRS complex, transthoracic EchoCG,Speckle-tracking EchoCG,Myocardial work, 6-minute walk test, determination of the level of Pro-natriuretic N-terminal peptide (NT-proBNP), Holter ECG, and a questionnaire based on the Minnesota quality of life questionnaire for patients with CHF (MHFLQ).
100 patients were enrolled sequentially,100 patients received only optimal drug therapy for chronic heart failure 100 patients ( Without Optimizer device ) with CHF and AF before study and after 2 and 6 и 12 months of follow-up: 12-channel ECG with an estimate of the width of the QRS complex, transthoracic EchoCG,Speckle-tracking EchoCG,Myocardial work, 6-minute walk test, determination of the level of Pro-natriuretic N-terminal peptide (NT-proBNP), Holter ECG, and a questionnaire based on the Minnesota quality of life questionnaire for patients with CHF (MHFLQ).