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Neutrophil dysfunction and sepsis in ICU patients.

Neutrophil dysfunction and sepsis in ICU patients. - NERTHUS-Study II

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31712
Enrollment
160
Registered
2006-12-12
Start date
2007-03-12
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

Trauma en acute post-operatieve patiënten multiple organ failure Sepsis

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) Patients admitted to the intensive care unit 2) After sugery or major trauma 3) Age above 18 4) Expected stay > 2 days

Exclusion criteria

Exclusion criteria: Immunological compromised - e.g. patients treated with steroids and/or cytostatic drugs

Design outcomes

Primary

MeasureTime frame
Primary variables: - Degree of inactivity of neutrophils Primary outcome: - Development of inflammatory-induced complications (sepsis/septic shock/(multiple) organ failure) (According to the SIRS/Sepsis criteria)

Secondary

MeasureTime frame
Secundary variables: - Normalization of neutrophil receptor profile - Percentage of cells in specific populations of neutrophils. Secundary outcome: - Development of inflammatory-induced complications (sepsis/septic shock/(multiple) organ failure) - Severity of illness during the intensive care period (According to disease severity on admission: APACHE II Score) (According to the maximal SOFA score during admission)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)