Platelet dysfunction at trauma patients

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00025434

Enrollment

700

Registered

2021-05-26

Start date

2021-05-26

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

D65

Interventions

Group 1: Retrospektive analysis of data: The correct parameters are documented upon admission to the emergency room: laboratory parameters (HB, BE, lactate), standard coagulation parameters (Qick, INR

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: - 18 years and older - medical care in the emergency room - Injury Severity Score (ISS) or New Injury Severity Score (NISS) =9

Exclusion criteria

Exclusion criteria: - Age <18 years - missing laboratory parameters

Design outcomes

Primary

Measure	Time frame
Platelet dysfunction at trauma patients when admitted to the emergency room, if the PFA-100 is used as a screening test (yes / no)?	—

Secondary

Measure	Time frame
Which predictors for platelet dysfunction at the trauma patient can be derived? Does a pathological PFA-100 value correlate with different ROTEM values (CT-Extem, CT-Internal, CT-Fibtem, MCF-Extem / Internal / Fibtem, etc.)? Transfusion needs of patients with proven platelet dysfunction vs. patients without this disorder.	—

Countries

Germany

Contacts

Public ContactPeter Hilbert-Carius

BG Klinikum Bergmannstrost Halle gGmbHKlinik für Anästhesiologie, Intensiv- und Notfallmedizin, Schmerztherapie

peter.hilbert@bergmannstrost.de0345 132 7716

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026