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临床试验/NCT04705688
NCT04705688招募中不适用

Platelet-activation and Optimal Inhibition in Patients With Atrial Fibrillation Undergoing Left Atrial Appendage Occlusion; The POPULAR-LAAO Trial

R&D Cardiologie1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2021年2月24日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
120
试验地点
1
主要终点
Change in coagulation activation

研究概览

简要总结

The POPULAR-LAAO registry is an open-label observational prospective registry to investigate hemostatic processes following left atrial appendage occlusion.

详细描述

This is an open-label observational prospective registry. The aim is to develop a better understanding of coagulation, platelet reactivity and prothrombotic factors in the first months after left atrial appendage occlusion, as occurrence of device-related thrombus and optimal postprocedural management remain a challenge after LAAO.

The study population will consist of patients with non-valvular atrial fibrillation (AF) at risk for cardio-embolic stroke scheduled for left atrial appendage occlusion. In these patients, blood samples for coagulation and platelet reactivity testing will be taken, which will be gathered prior to the procedure and 1 day, 14 days, 3 months and 6 months after the procedure. Data will be analyzed longitudinally and between groups based on patient characteristics.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The subject is aged 18 years or older
  • The subject is accepted/scheduled for left atrial appendage occlusion
  • The subject has a CHA₂DS₂-VASc Score ≥2 (male) or ≥3 (female)
  • The subject or legal representative is able to understand and is willing to provide written informed consent to participate in the trial.

排除标准

  • Unable or unwilling to return for required follow-up visits and examinations
  • Mechanical heart valves or valvular disease requiring surgery or interventional procedure
  • Ongoing major bleeding or complicated or recent (<72hours) major surgery
  • Known large oesophageal varices or decompensated liver disease (unless a documented positive opinion of a gastro-enterologist)
  • Severe thrombocytopenia (<50,000/ml)
  • High likelihood of being unavailable for follow-up or psycho-social condition making study participation impractical.
  • Woman with child bearing potential who do not use an efficient method of contraception.
  • Positive serum or urine pregnancy test for woman with child bearing potential
  • Pregnancy or within 48 hours post-partum
  • unsuitable LAA anatomy for occlusion or thrombus in the LAA at the time of procedure
  • contraindications or unfavourable conditions to perform cardiac catheterization or transesophageal echocardiography (TEE)
  • atrial septal malformations, atrial septal defect or a high-risk patent foramen ovale that may cause thrombo-embolic events
  • atrial septal defect repair or closure device or a patent foramen ovale repair or any other anatomical condition as this may preclude an LAAO procedure
  • Mitral valve regurgitation grade 3 or more
  • Aortic valve stenosis (AVA<1.0 cm2 or Pmax>50 mmHg) or regurgitation grade 3 or more
  • Planned carotid endarterectomy (CEA) for significant carotid artery disease
  • Life expectancy of less than 1 year

结局指标

主要结局

Change in coagulation activation

时间窗: Pre-LAAO and post-LAAO (1 day, 2 weeks, 3 months, 6 months)

Influence of LAAO on coagulation activation over time

Change in platelet reactivity

时间窗: Pre-LAAO and post-LAAO (1 day, 2 weeks, 3 months, 6 months)

Influence of LAAO on platelet reactivity over time

CYP2C19 genotype

时间窗: Pre-LAAO

Rate of clopidogrel non-responders among LAAO patients will be assessed by determining CYP2C19 genotype

次要结局

  • Device related thrombus event rate(Post-LAAO (3 months, 12 months))
  • Separate and composite event rates of stroke (ischemic or hemorrhagic), transient ischemic attack (TIA), systemic embolism and cardiovascular death.(Post-LAAO (3 months, 6 months, 12 months))
  • Major and minor bleeding event rate (according to Bleeding Academic Research Consortium criteria)(Post-LAAO (3 months, 6 months, 12 months))

研究者

发起方
R&D Cardiologie
申办方类型
Other
责任方
Principal Investigator
主要研究者

L.V.A. Boersma

Clinical professor

R&D Cardiologie

研究点 (1)

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