A pilotstudy to clinical scorings systems and biomarkers in blood and urine of sepsis patients in the emergency care

Completed

• Conditions: Sepsis; blood poisoning

• Registration Number: NL-OMON37120
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 160

Inclusion Criteria

Age > 18 year
Patients with suspected infection and two or more of the SIRS criteria [temperature <36*C or >38*C, heart rate > 90 beats/minute, respiratory rate >20 per minute, WBC > 12.000 or < 4000 cells/micro liter or pCO2 < 4.2 kPa] in the emergency department, who will be admitted to a ward or intensive care unit.
Informed consent.

Exclusion Criteria

Age <18 years, not admitted from the Emergency Care.

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main endpoints are mortality and clinical course of the admission. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary endpoint will be the development of acute kidney injury.</p><br>