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临床试验/NCT05155865
NCT05155865已完成不适用

Conduction System Pacing Versus Biventricular Pacing for Cardiac ResYNChronization (CSP-SYNC)

University Medical Centre Ljubljana2 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2022年1月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
62
试验地点
2
主要终点
Difference in 6-minute walk test distance

研究概览

简要总结

Cardiac resynchronization therapy (CRT) with biventricular pacing (BiV) is the cornerstone treatment for heart failure patients with ventricular dyssynchrony. Recently, a new concept, conduction system pacing (CSP) with permanent pacing, including His bundle pacing and left bundle branch pacing, has been proposed as a potential alternative to conventional BiV-CRT. The prospective, randomized trial will compare echocardiographic, electrocardiographic, and clinical effects of CSP versus conventional BiV pacing in heart failure patients with reduced ejection fraction (LVEF ≤ 35%), sinus rhythm, and left bundle branch block. Patients will be randomized to either CSP or biventricular pacing study group and followed up for at least 6 months. The study will explore whether CSP is non-inferior to BiV pacing in echocardiographic, electrocardiographic, and clinical outcomes.

详细描述

Cardiac resynchronization therapy (CRT) with biventricular pacing is an integral part of heart failure therapy in patients with reduced ejection fraction and wide QRS. Previous studies have demonstrated improved quality of life, reduced heart failure hospitalization, and decreased all-cause mortality. However, approx. 30% of patients still do not benefit from this therapy. High pacing thresholds and phrenic nerve stimulation are also common problems with BiV stimulation. Newer CRT systems with improved programmability and algorithms in conjunction with quadripolar left ventricular leads have solved some challenges of BiV pacing. However, BiV stimulation with non-physiological epicardial activation has shown a possible pro-arrhythmic effect which is more pronounced in the non-responder population.

On the other hand, CSP provides synchronous physiological ventricular activation with possible superior electrical and mechanical resynchronization compared to BiV pacing. Electrical activation maps obtained during CSP showed normalization of left bundle branch block with more homogeneous electrical resynchronization than in biventricular pacing. Additionally, BiV CRT effectively corrects mechanical dyssnchrony, demonstrated with homogenization of myocardial work. This has already been proven as the underlying pathophysiological mechanism for successful CRT response. However, the effect of CSP on echocardiographic parameters of mechanical dyssynchrony is not known.

Previous studies of CSP focused on feasibility and its benefits over right ventricular pacing in patients with refractory atrial fibrillation who underwent atrioventricular node ablation and pacemaker implantation. Promising results were followed by the acknowledgment of this physiological mode of pacing by the recent guidelines of European Society of Cardiology. However, studies evaluating the value of CSP as an alternative approach to BiV CRT in heart failure patients are limited. The purpose of this study is to compare the effects of CSP and conventional BiV pacing on electrocardiographic and echocardiographic parameters as well as on clinical outcomes in patients with heart failure with reduced ejection fraction (LVEF ≤35%), sinus rhythm, and left bundle branch block. In this single-center study, 60 patients will be randomized into one of two arms: a BiV pacing arm with BiV CRT implantation based on clinical guidelines or an experimental CSP arm with the implantation of a CSP device. Device with a defibrillator (ICD) will be selected at the discretion of the implanting physician. Baseline and follow up assessments will include clinical evaluation (New York Heart Association class, 6-minute walking distance), evaluation of quality of life (EQ-5D index), laboratory tests (N-terminal pro-B-type natriuretic peptide), electrocardiographic recordings (standard 12-leads ECG and high-resolution-ECG), and echocardiographic evaluation (standard echocardiographic parameters of LV reverse remodeling and non-invasive myocardial work assessment). Intra-operative and procedural parameters will also be recorded.

Investigators hypothesize that CSP could represent a feasible and safe alternative to conventional BiV pacing in terms of clinical, electrocardiographic, and echocardiographic outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The proposed inclusion criteria represent the minimum recommendations for CRT implantation according to the ESC 2021 guidelines. In addition:
  • Sinus rhythm and complete left bundle branch block according to Strauss criteria
  • NYHA class II-III
  • Optimal medical heart failure therapy for at least 3 months before enrollment
  • The patient is able to understand and willing to provide a written informed consent
  • 18 years of age or older

排除标准

  • Mechanical tricuspid valve replacement
  • More than moderate valvular disease
  • Unstable angina, acute MI, CABG, or PCI within the past 6 months
  • Persistent or permanent atrial fibrillation
  • Ventricular arrhythmias (frequent PVC) which do not allow to acquire consecutive regular beats during echocardiography and electrocardiography
  • Higher degree AV block
  • Life expectancy of less than 12 months
  • Pregnancy and breastfeeding
  • Acute illness or active systemic infection

结局指标

主要结局

Difference in 6-minute walk test distance

时间窗: 6 months

meters

Change in left ventricular volume

时间窗: acute after the procedure, 1 month, 6 months, 12 months

Effect on reverse left ventricular remodeling measured as changes in left ventricular volume in both arms

Difference in pro-BNP value

时间窗: 6 months

pg/mL

Difference in the EQ-5D index

时间窗: 6 months

score

Change in left ventricular ejection fraction

时间窗: acute procedure, 1 month, 6 months, 12 months

Effect on reverse left ventricular remodeling measured as changes in left ventricular ejection fraction in both arms

Difference in Heart Failure Class

时间窗: 6 months

From class 1 to 4

次要结局

  • Rate of procedural complications(at least 12 months after enrollment)
  • Difference in QRS complex width(acute after the procedure, 1 month, 6 months, 12 months)
  • Difference in myocardial work redistribution(acute after the procedure, 1 month, 6 months, 12 months)
  • Difference in arrhythmia occurrence(at least 12 months after enrollment)
  • Difference in sum absolute QRST integral(acute after the procedure, 1 month, 6 months, 12 months)
  • Tpeak-end duration(acute after the procedure, 1 month, 6 months, 12 months)
  • Difference in filtered QRS duration on high-resolution electrocardiogram(acute after procedure, 1 month, 6 months, 12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

David Žižek, MD, PhD

assist. prof. David Žižek, MD, PhD

University Medical Centre Ljubljana

研究点 (2)

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