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Clinical Trials/NCT06523075
NCT06523075
Completed
Not Applicable

Construction and Validation of a Sepsis Prediction Model Based on Dysregulation of Host Response

Second Affiliated Hospital of Wenzhou Medical University2 sites in 1 country1,000 target enrollmentSeptember 1, 2024
ConditionsSepsis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sepsis
Sponsor
Second Affiliated Hospital of Wenzhou Medical University
Enrollment
1000
Locations
2
Primary Endpoint
Sepsis
Status
Completed
Last Updated
last year

Overview

Brief Summary

The aim of this study is to identify risk factors associated with sepsis and to construct a predictive model for sepsis. This will provide an objective theoretical and empirical foundation for the diagnosis, assessment, and management of sepsis in our country.The primary questions addressed are:

What are the risk factors for the development of sepsis? How do we improve the prognosis of sepsis?

Registry
clinicaltrials.gov
Start Date
September 1, 2024
End Date
October 17, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Second Affiliated Hospital of Wenzhou Medical University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with Infection or Suspected Infection

Exclusion Criteria

  • Patients with Autoimmune Diseases
  • Pregnant Women
  • Patients with Advanced-Stage Cancer and Systemic Metastasis

Outcomes

Primary Outcomes

Sepsis

Time Frame: 3 months

A rapid increase of 2 or more points points in the Sequential Organ Failure Assessment (SOFA) score after patient infection.SOFA score, which ranges from a minimum of 2 to a maximum of 15, indicates a worse outcome with higher scores.

Study Sites (2)

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