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Biomarkers of Sepsis

Biomarkers of Sepsis - Biomarkers of Sepsis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36012
Enrollment
500
Registered
2011-09-09
Start date
2011-10-13
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

blood poisoning sepsis

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Age > 18 years - Presence of an arterial line - Patients who score positive for sepsis according to the Bone criteria (at least 2 SIRS criteria plus clinical suspicion of infection).

Exclusion criteria

Exclusion criteria: - No informed consent. - Patients receiving > 48 hours of antibiotic treatment for a suspected infection prior to ICU admission. - Previous participation in this study.

Design outcomes

Primary

MeasureTime frame
Endpoints include pathogen etiology, systemic inflammatory parameters and MODS. The endpoints will enable us to develop a predictive model for risk stratification for sepsis and provides insight in the pathophysiologic processes of sepsis and might lead to novel therapeutic interventions.

Secondary

MeasureTime frame
nvt

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)