sepsis prediction in trauma patients

sepsis prediction in trauma patients - SPrinT

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00010991

Enrollment

100

Registered

2016-11-15

Start date

2015-01-01

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

T07 R65

Interventions

Group 1: The course of biomarker CRP, PCT, IL-6, CLI and Presepsin following severe trauma

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: severe trauma (ISS>16), admission to ICU

Exclusion criteria

Exclusion criteria: chronical infections (Hepatitis, HIV)

Design outcomes

Primary

Measure	Time frame
biomarker CRP, PCT, CLI and presepsin concentration on time of admission and following 7 days in blood sample	—

Secondary

Measure	Time frame
icu discharge (as well as death) on day 1 to 7	—

Countries

Germany

Contacts

Public ContactSophie Ruhrmann

Universitätsklinikum Gießen und Marburg,Klinik für Anästhesie, Intensivmedizin und Schmerztherapie

sophie.ruhrmann@chiru.med.uni-giessen.de004964198544401

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 21, 2026