Response of Intracardiac Thrombus to Anticoagulants in Patients With Non-valvular Atrial Fibrillation (LYSIS)

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorFirst Affiliated Hospital Xi'an Jiaotong University

About this trial

This study aims to analyze changes in the immune status, metabolic status, and host microbiome community structure in non-valvular atrial fibrillation patients with intracardiac thrombus. Additionally, the study aims to analyze factors that influence the responsiveness and occurrence of adverse events related to anticoagulant therapy.

Eligibility criteria

Qualifiers

Age ≥18 years old, age ≤80 years old

Patients with atrial fibrillation detected by routine surface 12-lead electrocardiography or Holter

Transesophageal echocardiography confirmed the presence of cardiac thrombus, and the patient had not received any anticoagulant therapy

Disqualifiers

Echocardiography confirmed valvular heart disease

Contraindications to anticoagulants

Patients with the previous history of hemorrhagic stroke

Low platelet count or functional platelet defects

Trial design

Treatments tested in this trial

  • Observational; No Interventions were given.

Treatment groups

500 Participants
are divided into 2 treatment groups

Sponsors and collaborators

First Affiliated Hospital Xi'an Jiaotong University

Lead sponsor

521 Hospital of NORINCO Group

Collaborator

Shaanxi Provincial People's Hospital

Collaborator

Xiangyang Central Hospital

Collaborator

Henan Provincial People's Hospital

Collaborator