Last updated: November 20, 2023
Sponsor: Tomsk National Research Medical Center of the Russian Academy of Sciences
Overall Status: Active - Recruiting
Phase
N/A
Condition
Heart Failure
Heart Attack (Myocardial Infarction)
Coronary Artery Disease
Treatment
Implantation of Cardioverter-defibrillator with a Resynchronization Function Using Left Bundle Branch Pacing
Implantation of Cardioverter-defibrillator with a Resynchronization Function Using Biventricular Pacing
Clinical Study ID
NCT05769036
RECOVER-HF
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion criteria:
- The patient is willing and able to comply with the protocol and has provided writteninformed consent;
- Male or female patients aged 18 to 80 years;
- Patients with ischemic or non-ischemic cardiomyopathy;
- Symptomatic HF for at least 3 months prior to enrollment in the study;
- New York Heart Association (NYHA) functional class HF ≥ II;
- Patients with HF in sinus rhythm (SR) with LVEF ≤ 35% (measured in the last 6 weeksprior to enrollment), QRS duration ≥150 ms with LBBB morphology;
- Patients with HF in SR with LVEF ≤ 35% (measured in the last 6 weeks prior toenrollment), QRS duration 130-149 ms with LBBB morphology;
- Patients with HF in SR with LVEF ≤ 35% (measured in the last 6 weeks prior toenrollment), QRS duration ≥150 ms with non-LBBB morphology;
- Patients with symptomatic persistent or permanent atrial fibrillation, HF with LVEF < 40% (measured in the last 6 weeks prior to enrollment) and an uncontrolled heart ratewho are candidates for atrioventricular junction ablation (irrespective of QRSduration);
- Patients with HF, LVEF < 40% (measured in the last 6 weeks prior to enrollment) andindications for continuous ventricular pacing due to bradycardia;
- Patients who have received a conventional pacemaker or an implantedcardioverter-defibrillator and who subsequently develop symptomatic HF with LVEF < 40% (measured in the last 6 weeks prior to enrollment) despite optimal medical therapy,and who have a significant proportion of right ventricle pacing;
- Optimal HF medical therapy.
Exclusion
Exclusion criteria:
- Coronary artery (CA) bypass grafting, balloon dilatation or CA stenting within 3months prior to enrollment;
- Acute myocardial infarction within 3 months prior to enrollment;
- Acute coronary syndrome;
- Patients with planned cardiovascular intervention (CA bypass grafting, balloondilatation or CA stenting);
- Patients listed for heart transplant;
- Patients with implanted cardiac assist device;
- Acute myocarditis;
- Infiltrative myocardial disease;
- Hypertrophic cardiomyopathy;
- Severe primary stenosis or regurgitation of the mitral, tricuspid and aortic valves;
- Woman currently pregnant or breastfeeding or not using reliable contraceptive measuresduring fertility age;
- Mental or physical inability to participate in the study;
- Patients unable or unwilling to cooperate within the study protocol;
- Patients with rheumatic heart disease;
- Mechanic tricuspid valve patients;
- Patients with any serious medical condition that could interfere with this study;
- Enrollment in another investigational drug or device study;
- Patients not available for follow-up;
- Patients with severe chronic kidney disease (estimated glomerular filtration rate ˂ 30ml/min/1.73 m2);
- Life expectancy ≤ 12 months;
- Participation in another telemonitoring concept.
Study Design
Total Participants: 60
Treatment Group(s): 2
Primary Treatment: Implantation of Cardioverter-defibrillator with a Resynchronization Function Using Left Bundle Branch Pacing
Phase:
Study Start date:
October 01, 2023
Estimated Completion Date:
September 01, 2028
Study Description
Connect with a study center
Cardiology Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences
Tomsk,
Russian FederationActive - Recruiting
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