NCT05965375

Risk Stratification Value of Biomarkers in Patients With Ventricular Arrhythmias

Risk Stratification Value of Biomarkers in Patients With Ventricular Arrhythmias (FUTURE): an Investigator-initiated, National, Multicenter, Retrospective-prospective, Cohort Study
First Affiliated Hospital Xi'an Jiaotong University·ClinicalTrials.gov·otherNot yet recruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Ventricular Arrythmia
Drug/Device/Intervention
Observational; No Interventions were given.
Study type
Observational
Intervention type
other
Sponsor & location
Primary sponsor
First Affiliated Hospital Xi'an Jiaotong University
Location
Xi'an, China
Timeline & enrollment
Phase
N/A
Start date
Oct 31, 2023
End date
May 31, 2027
Enrollment
5000 participants
Primary outcome

Change in the incidence of MACCE

Summary

The investigation of biomarkers for immune status and metabolic state, as well as host
 microbiota composition, in patients with ventricular arrhythmias before and after
 radiofrequency ablation, can provide new insights for specific and personalized treatment.
 This can help establish early prediction and prognosis models and provide a basis for
 clinically effective diagnosis and treatment.

ICD-10 classifications
Ventricular tachycardiaLeft ventricular failureVentricular septal defectCardiomyopathy, unspecifiedCardiac arrhythmia, unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05965375
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05965375 through Pure Global AI's free database. This phase not specified trial is sponsored by First Affiliated Hospital Xi'an Jiaotong University and is currently Not yet recruiting. The study focuses on Ventricular Arrythmia. Target enrollment is 5000 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.