Risk Stratification Value of Biomarkers in Patients With Ventricular Arrhythmias

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

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with ventricular premature beats, ventricular tachycardia, or ventricular fibrillation detected by regular surface twelve-lead electrocardiogram or Holter.

Disqualifiers

Age <18 or >80 years old;

Patients with autoimmune diseases or immune deficiencies, or those who have used immunosuppressive or immune modulating agents in the past 3 months;

Platelet count <100×10^9/L or functional platelet defects;

Congenital or acquired coagulation or bleeding disorders;

Trial population

Patients with ventricular premature beats, ventricular tachycardia, or ventricular fibrillation detected by regular surface twelve-lead electrocardiogram or Holter.

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

  • Observational; No Interventions were given.

    Other intervention

    Observational; No Interventions were given.

Treatment groups

5,000 Participants
are divided into 5 treatment groups
Group A: Occasional premature ventricular contractions group1 intervention
Group B: Frequent premature ventricular contractions group1 intervention
Group C: Short runs of ventricular tachycardia group1 intervention
Group D: Sustained ventricular tachycardia group1 intervention
Group E: Ventricular fibrillation group1 intervention

Trial outcomes

Primary outcomes

1

Change in the incidence of MACCE

Major adverse cardiovascular and cerebrovascular events, including myocardial infarction, stroke, vessel revascularization and all-cause death. The MACCE will be assessed from the medical records.

Time frame
3,6 months,1,3,5 years after enrollment.

Secondary outcomes

1

Change in the incidence of myocardial infarction

Myocardial infarction diagnosed by clinical doctors will be assessed from the medical records.

Time frame
3,6 months,1,3,5 years after enrollment.
2

Change in the incidence of stroke

Stroke diagnosed by clinical doctors will be assessed from the medical records.

Time frame
3,6 months,1,3,5 years after enrollment.
3

Change in the incidence of vessel revascularization

Vessel revascularization assessed by clinical doctors will be assessed from the medical records.

Time frame
3,6 months,1,3,5 years after enrollment.
4

Change in the incidence of all-cause death

All-cause death diagnosed by clinical doctors will be assessed from the medical records.

Time frame
3,6 months,1,3,5 years after enrollment.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

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

This trial is not recruiting at the moment. You can still explore other options: