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临床试验/NCT07257614
NCT07257614
尚未招募
不适用

Left Atrial Appendage Occlusion in Dialysis Patients With Atrial Fibrillation: A Multicentre Pilot Study

Prince of Wales Hospital, Shatin, Hong Kong1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年1月5日最近更新:

概览

阶段
不适用
状态
尚未招募
发起方
Prince of Wales Hospital, Shatin, Hong Kong
入组人数
40
试验地点
1
主要终点
1 year transient ischemic attack

概览

简要总结

Objectives: This pilot study aims to evaluate the safety and efficacy of left atrial appendage occlusion (LAAO) in dialysis patients and atrial fibrillation (AF) to establish a novel stroke prevention strategy and determine an optimal post-occlusion antithrombotic regime. Page 3 of 50 Hypothesis: The study tests the hypotheses that LAAO is safe for dialysis patients, that a single antiplatelet regimen postprocedure is safe, and that LAAO effectively reduces the composite endpoint of stroke/transient ischemic attack and major bleeding compared to standard care. Instruments: The study employs a multicenter, single-arm prospective registry design. Eligible participants, aged ≥18 with documented AF and ESRF on peritoneal dialysis (PD) or hemodialysis (HD), will undergo LAAO using the Watchman Flx PRO device. Propensity score matched historical cohort from dialysis registry will be identified for comparison.

Main Outcome Measures: The primary endpoint is the composite of stroke/transient ischemic attack/systemic embolism and non-procedural-related major bleeding at one year. Secondary endpoints include individual rates of these events, procedural safety and device occlusion effectiveness. Data Analysis and Expected Results: Statistical analysis will involve descriptive statistics, chi-squared tests, and propensity score matching. A p-value of <0.05 will be deemed significant. The pilot study anticipates a low peri-procedural complication rate (≤5%) and confirms LAAO's efficacy in stroke and major bleeding reduction in Chinese PD and HD patients compared to standard care. This data will inform the design of a larger randomized controlled trial aimed at validating LAAO as a safe alternative for AF management in dialysis populations.

研究设计

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

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

  • Age \>=18
  • End stage renal failure on peritoneal dialysis or haemodialysis
  • documented paroxysmal, persistent, or permanent non-valvular atrial fibrillation;
  • CHADS2-VASc \>=2
  • The patient is willing and able to comply with the required medication post-procedure and follow-up evaluations;
  • Able to consent

排除标准

  • Patients who require long-term anticoagulation for a condition other than AF, e.g. pulmonary embolism, deep vein thrombosis, anti-phospholipid syndrome
  • Mechanical valve replacement
  • Active infection with bacteraemia;
  • Pregnant or nursing patients and those who plan pregnancy during the study period. Female patients of childbearing potential must have a negative pregnancy
  • Known hypersensitivity or contraindication to aspirin, clopidogrel, heparin, any device material or component (nickel titanium, PET, polypropylene), and/or contrast;
  • Left atrial appendage is obliterated and surgical ligated;
  • Underwent any cardiac or non-cardiac interventional or surgical procedure within 30 days prior to the procedure or planned to have the interventional or surgical procedure within 60 days after implant procedure (e.g., cardioversion, ablation, percutaneous coronary intervention, etc.);
  • Recent (within 90 days prior to procedure) stroke, transient ischemic attack, or myocardial infarction;
  • New York Heart Association Class IV;
  • Life expectancy is less than 1 year;

结局指标

主要结局

1 year transient ischemic attack

时间窗: 1 year

Rate of transient ischemic attack in enrolled patient at 1 year

1 year stroke rate

时间窗: 1 year

Stroke rate of enrolled cases at 1-yera follow-up

1 year major bleeding rate

时间窗: 1 year

Rate of major bleeding (BRAC 3-5) of enrolled cases at 1-year follow-up

次要结局

  • 1 year minor bleeding rate(1 year)
  • 1 year systemic embolism rate(1 year)
  • LAAO safety endpoint(7 days post-discharge)
  • LAAO effectiveness endpoint(1 year)
  • Peri-device leak rate at 1 month(1 month)
  • Rate of device endotheliasation at 3 month(3 month)
  • Rate of device endotheliasation at 12 month(12 month)
  • Rate of 1-year cardiovascular mortality at 12 month(12 month)
  • Device Related Thrombus rate at 1 month(1 month)
  • Rate of device endotheliasation at 1 month(1 month)
  • Comparison of outcome between prospective and retrospective group(12 month)

研究者

发起方
Prince of Wales Hospital, Shatin, Hong Kong
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr So Chak Yu kent

Clinical Assistant Professor

Prince of Wales Hospital, Shatin, Hong Kong

研究点 (1)

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