About this trial

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.

Eligibility criteria

Qualifiers

Age >=18

End stage renal failure on peritoneal dialysis or haemodialysis

documented paroxysmal, persistent, or permanent non-valvular atrial fibrillation;

CHADS2-VASc >=2

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

40 Participants
are grouped into 2 trial groups

Locations

1
The Chinese Universityy of Hong Kong ShatinNew Territories, Hong Kong

Sponsors and collaborators

Prince of Wales Hospital, Shatin, Hong Kong

Lead sponsor

The Queen Elizabeth Hospital

Collaborator

Pok Oi Hospital

Collaborator

Tuen Mun Hospital

Collaborator

Princess Margaret Hospital, Hong Kong

Collaborator

Alice Ho Miu Ling Nethersole Hospital

Collaborator

Kiang Wu Hospital

Collaborator