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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05309889
Other study ID # SYSEC-KY-KS-2022-009
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 12, 2022
Est. completion date June 2023

Study information

Verified date March 2022
Source Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Contact Yuewei Li
Phone 020-81332587
Email liyw7@mail2.sysu.edu.cn
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Sepsis is a life-threatening organ dysfunction caused by a dysregulated host response to infection and is associated with high morbidity and mortality. Sepsis3 gives sepsis a broad definition, reflecting the heterogeneity of the disease. So we need a precise treatment with a stratification of patient prognosis in order to reduce mortality in patients with sepsis.


Recruitment information / eligibility

Status Recruiting
Enrollment 174
Est. completion date June 2023
Est. primary completion date May 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients who met the Sepsis3 diagnostic criteria. Exclusion Criteria: - Absence of laboratory test items (blood routine examination, coagulation function, liver function, biochemistry, urine routine examination, urine renal function, urine protein, etc.) >20%. - Admission in ICU less than 48 hours. - Patient with psychiatric disorders. - Under 18 years of age.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
no intervention
no intervention

Locations

Country Name City State
China Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University Guangzhou

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary mortality rate all-cause deaths that occurred in 28 days 28 days after diagnosis of sepsis
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