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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05965362
Other study ID # XJTU1AF2023LSK-151
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date December 31, 2024
Est. completion date December 31, 2028

Study information

Verified date March 2024
Source First Affiliated Hospital Xi'an Jiaotong University
Contact Guoliang Li
Phone +8613759982523
Email liguoliang_med@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

Infective endocarditis is an inflammation of the inner lining of the heart valves or ventricular walls caused by direct infection of the heart by bacteria, fungi and other microorganisms via the bloodstream route. At present, the clinical diagnosis of IE is mainly based on a combination of typical symptoms, imaging and blood culture, etc. Finding more sensitive means and more accurate indicators for early detection of IE flora distribution characteristics is of great significance for the prevention and targeted treatment of IE. Therefore, 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 2000
Est. completion date December 31, 2028
Est. primary completion date December 31, 2028
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with clinically confirmed infective endocarditis Exclusion Criteria: - Patients refuse to sign informed consent form - Patients who combined with serious systemic diseases, cannot tolerate the acquisition of biological samples

Study Design


Intervention

Other:
Observational; No Interventions were given.
Observational; No Interventions were given.

Locations

Country Name City State
China First Affiliated Hospital of Xian Jiantong University Xi'an Shaanxi

Sponsors (5)

Lead Sponsor Collaborator
First Affiliated Hospital Xi'an Jiaotong University 521 Hospital of NORINCO Group, Henan Provincial People's Hospital, Shaanxi Provincial People's Hospital, Xiangyang Central Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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. 1, 3, 6 months and 1, 2, 3, 5 years after enrollment.
Secondary Incidence of adverse thrombus complications Adverse thrombus complications including systemic embolism, infected aneurysm, splenic abscess, etc. 5 years after the enrollment.
Secondary Change in the incidence of infection recurrence Diagnosis of infective endocarditis by clinical guidelines, which will be assessed from medical records. 1, 3, 6 months and 1, 2, 3, 5 years after enrollment.
Secondary Change in the incidence of myocardial infarction Myocardial infarction, diagnosed by clinical doctors, will be assessed from medical records. 1, 3, 6 months and 1, 2, 3, 5 years after enrollment.
Secondary Change in the incidence of stroke Stroke, diagnosed by clinical doctors, will be assessed from medical records. 1, 3, 6 months and 1, 2, 3, 5 years after enrollment.
Secondary Change in the incidence of vessel revascularization Vessel revascularization, diagnosed by clinical doctors, will be assessed from medical records. 1, 3, 6 months and 1, 2, 3, 5 years after enrollment.
Secondary Change in the incidence of all-cause death All-cause death, diagnosed by clinical doctors, will be assessed from medical records. 1, 3, 6 months and 1, 2, 3, 5 years after enrollment.
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