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临床试验/NCT04165642
NCT04165642终止不适用

Single-Laser PVI: Single-encirclement Laserballoon Ablation for Pulmonary Veins Isolation

IRCCS Policlinico S. Donato1 个研究点 分布在 1 个国家目标入组 82 人开始时间: 2019年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
82
试验地点
1
主要终点
Success rate at 1 year

研究概览

简要总结

To assess the efficacy of laser balloon ablation of atrial fibrillation (AF) without verification of electrical isolation of pulmonary veins using implantable loop recorder.

This is a prospective and single-center study. A targeted number of 82 patients suffering from paroxysmal or persistent AF, indicated to undergo catheter ablation will be included. The study will consist of: i) patient enrolment, ii) treatment phase, and iii) 1-year follow-up phase. The duration of the study is expected to be 24 months, from first patient enrolment to last patient follow up.

详细描述

This is a prospective and single-center study. A targeted number of 82 patients suffering from paroxysmal or persistent AF, indicated to undergo catheter ablation will be included. The study will consist of: i) patient enrolment, ii) treatment phase, and iii) 1-year follow-up phase. The duration of the study is expected to be 24 months, from first patient enrolment to last patient follow up.

In a recent meta-analysis including 1188 patients, free from arrhythmic recurrences at 12 months after a single ablative procedure with a laser balloon and without continuous monitoring with ILR was 74%1.

Assuming that the approach without post-ablative verification of pulmonary vein isolation and continuous monitoring with ILR can lead to a 60% success rate at 12 months, 80 patients are required to have an 80% probability to observe a level of 2-code significance of 0.05 in an exponential model with the log rank test. With an estimated loss of data (patients lost to follow-up, protocol deviations and incomplete data) of 5%, the total number of patients to be enrolled is 82.

Subject screening and enrolment will be carried out for approximately 12 months. The study will continue up to 12 months after last patient enrolment, dependent on the rate of enrolment and the regulatory timeline (as applicable).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • To participate in this clinical subject, the subject must meet all of the following inclusion criteria:
  • Age between 18 and 85 years
  • Paroxysmal or persistent AF
  • Patients AF who have indications for the first time ablation procedure according to the ESC / EHRA recommendations (European Society of Cardiology / European Heart Rhythm Association).
  • Ability to provide written informed consent for study participation and be willing and able to comply with the study evaluations and follow up schedule

排除标准

  • Subjects are not eligible for clinical study participation if they meet any of the following exclusion criteria:
  • Previous AF ablation procedures
  • Secondary AF due to other causes
  • Hyperthyroidism
  • Left ventricular ejection fraction <30%
  • NYHA class IV
  • Left atrium area > 35 cm2
  • Severe disease of cardiac valves
  • Contraindication to anticoagulant therapy
  • Presence of thrombus in the left atrium
  • Myocardial infarction or unstable angina or recent coronary artery bypass (<6 months)
  • Thoracic surgery for congenital, valvular or aortic disease
  • History of cerebrovascular events
  • Pregnancy
  • Significant comorbidity, such as cancer, severe kidney failure requiring dialysis, severe obstructive pulmonary disease, cirrhosis, with a life expectancy of less than 2 years
  • Contraindications are present as indicated in the "instructions for use" of the devices used

结局指标

主要结局

Success rate at 1 year

时间窗: 12 months after ablation

Free from AF, atrial tachycardia and flutter documented with ILR or Holter ECG monitorwithout antiarrhythmic drugs.

次要结局

  • Procedural and 1-year complications related to the ablation procedure.(during the procedure and 12 months after ablation)
  • inducibility of AF after the procedures(During the procedure)
  • AF Burden(12 months after ablation)

研究者

发起方
IRCCS Policlinico S. Donato
申办方类型
Other
责任方
Principal Investigator
主要研究者

Carlo Pappone

Chief of the Department of Arrhythmology and Electrophysiology

IRCCS Policlinico S. Donato

研究点 (1)

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