Sepsis: From Syndrome to Personalized Care

Status Recruiting

Clinical Trial Summary

This is a prospective, observational study designed to examine the performance of biomarkers, molecular biological methods and other analysis in blood from patient with suspected sepsis in the Emergency department, as well as identidying novel sepsis endotypes. Around 1500 patients will be enrolled.

Clinical Trial Description

The study will prospectively include adult patients (>18 years) with suspected sepsis admitted to Oslo University Hospital, Ullevål (OUH-Ullevål). Patients admitted to the emergency department and managed by the medical rapid response team or the sepsis rapid response team are considered eligible for inclusion. Informed consent will be collected at the emergency department if possible, or within few days, by a clinical investigator or a study nurse. The investigators aim to include 1500 patients treated by the Sepsis Rapid Response Team or Medical Emergency team for possible sepsis. Patients classified to have had other conditions than sepsis in the post hoc assessment will be used as controls. The inclusion period will be 3 years. ;

Study Design

Related Conditions & MeSH terms

Sepsis
Sepsis Syndrome
Sepsis, Severe
Septic Shock
Syndrome
Systemic Inflammatory Response Syndrome
Toxemia

Clinical Trial Details

NCT number	NCT04203979
Study type	Observational [Patient Registry]
Source	Oslo University Hospital
Contact	Aleksander R Holten, PhD
Phone	+4799275784
Email	aleksander.holten@gmail.com
Status	Recruiting
Phase
Start date	January 6, 2020
Completion date	December 31, 2026

View Details

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