Clinical Trials Directory

Trials / Unknown

UnknownNCT05911711

Identification and Clinical Efficacy Analysis of Biomarkers in Sepsis Patients

Status
Unknown
Phase
Study type
Observational
Enrollment
120 (estimated)
Sponsor
Kangdong Sacred Heart Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Sepsis, a severe response to bacterial infection, lacks understanding of immunometabolic features that can identify high-risk patients. This study aimed to discover immune, biological, and metabolic biomarkers in sepsis patients with poor prognosis and understand the underlying mechanisms of host immune responses.

Detailed description

Sepsis is a life-threatening condition resulting from a dysregulated host response to infection and remains a significant global health crisis. Accurately identifying high-risk patients and understanding the underlying mechanisms of distinct host responses are crucial. Dysregulation of immune and biological responses, along with metabolic remodeling, has emerged as a prevalent characteristic in sepsis patients. However, there is still a need for a comprehensive understanding of specific markers related to immunometabolism and the underlying mechanisms contributing to the disturbance in sepsis pathogenesis. This study aims to investigate the immune, biological, and metabolic profiles of sepsis patients, focusing on the alteration of metabolism in sepsis patients with poor outcomes. The findings of this study will provide valuable insights into dysregulated immunometabolism, shedding light on its contribution to the potentiation of immunopathogenesis in sepsis. Eligibility Criteria adults over the age of 19 a sepsis patient in ICU Patients are excluded from the study If the patient or care giver does not agree to participate in the study a bone marrow transplant or an organ transplant patient a Do not resuscitation(DNR) patient a patient under the age of 18 Outcome Measure ICU mortality, 28 days mortality Use of inotropics, vasopressors CRRT(continuous renal replacement therapy), ECMO (Extracorporeal membrane oxygenation), Interventional lung assist, polymyxin

Conditions

Interventions

TypeNameDescription
OTHERPrognostic factornormal person (no sepsis group)

Timeline

Start date
2023-07-07
Primary completion
2023-12-31
Completion
2024-06-07
First posted
2023-06-22
Last updated
2023-06-22

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT05911711. Inclusion in this directory is not an endorsement.