Prognosis of Patients With Infective Endocarditis and Risk Stratification Value of Biomarkers (ENDEAVOR)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorFirst Affiliated Hospital Xi'an Jiaotong University

About this trial

In this study, by establishing a clinical cohort of infective endocarditis, we observed the natural prognosis and influencing factors in the process of disease development and regression; we used multi-omics technology to understand the prognostic value of its biomarkers, and provided new ideas and evidence for the pathogenesis, clinical diagnosis and treatment of IE.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with clinically confirmed infective endocarditis

Disqualifiers

Patients refuse to sign informed consent form

Patients who combined with serious systemic diseases, cannot tolerate the acquisition of biological samples

Trial population

Patients with clinically confirmed infective endocarditis

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

2,000 Participants
are divided into 1 treatment group
Group A: Infective endocarditis group1 intervention

Trial outcomes

Primary outcomes

1

Change in the incidence of MACCE

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

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

Secondary outcomes

1

Incidence of adverse thrombus complications

Adverse thrombus complications including systemic embolism, infected aneurysm, splenic abscess, etc.

Time frame
5 years after the enrollment.
2

Change in the incidence of infection recurrence

Diagnosis of infective endocarditis by clinical guidelines, which will be assessed from medical records.

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

Change in the incidence of myocardial infarction

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

Time frame
1, 3, 6 months and 1, 2, 3, 5 years after enrollment.
4

Change in the incidence of stroke

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

Time frame
1, 3, 6 months and 1, 2, 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