Automated immune phenotyping and priming of neutrophils in a trauma cohort

Automated immune phenotyping and priming of neutrophils in a trauma cohort - Automated immune phenotyping in trauma

Status

Active, not recruiting

Phases

Phase 2

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON46591

Enrollment

150

Registered

2018-10-31

Start date

2018-11-26

Completion date

Unknown

Last updated

2025-09-15

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

Conditions

trauma accident Trauma

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All trauma patients presented at the trauma bay in the emergency department of the UMCU, that need to undergo blood sampeling. Age must be at least 18.

Exclusion criteria

Exclusion criteria: Patient transferred from other hospitals to the UMC Utrecht.

Design outcomes

Primary

Measure	Time frame
Primary endpoint is reached if the following criteria are met: - The Trauma surgeon (or assistant) is able to perform all the necessary actions to start the blood analysis. - Blood analysis was started	—

Secondary

Measure	Time frame
The secondary endpoint is defined as a difference in neutrophil phenotype and/or response between the patients that develop infectious complications and non-infectious trauma patients.	—

Countries

Netherlands

Outcome results