Viewing Study NCT06141538



Ignite Creation Date: 2024-05-06 @ 7:48 PM
Last Modification Date: 2024-10-26 @ 3:14 PM
Study NCT ID: NCT06141538
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-04-04
First Post: 2023-11-15

Brief Title: Response of Intracardiac Thrombus to Anticoagulants in Patients With Non-valvular Atrial Fibrillation LYSIS
Sponsor: First Affiliated Hospital Xian Jiaotong University
Organization: First Affiliated Hospital Xian Jiaotong University

Study Overview

Official Title: Response of Intracardiac Thrombus to Anticoagulants in Patients With Non-valvular Atrial Fibrillation LYSIS an Investigator-initiated National Multicenter Retrospective-prospective Observational Cohort Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: LYSIS
Brief Summary: 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
Detailed Description: The researcher-initiated clinical cohort study is a national multicenter retrospective-prospective study of non-valvular atrial fibrillation patients with intracardiac thrombus based on molecular biology and multi-omics analysis The study aims to analyze the changes in the bodys immune status metabolic status and host microbiome community structure as well as to analyze the factors that influence the responsiveness of intracardiac thrombus to anticoagulant therapy The study also evaluates the occurrence of adverse events related to anticoagulation in these patients

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None