A multicenter, prospective observational study for the epidemiology of severe trauma

A multicenter, prospective observational study for the epidemiology of severe trauma - Epidemiology of severe trauma

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000019588

Enrollment

500

Registered

2015-11-15

Start date

2016-02-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Trauma

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Injury Severity Score >15

Exclusion criteria

Exclusion criteria: Out of hospital cardiac arrest

Design outcomes

Primary

Measure	Time frame
28-day mortality	—

Secondary

Measure	Time frame
ICU free days Ventilator free days 24-hour amount of blood transfusion Subsequent Acute Respiratory Distress Syndrome (ARDS)	—

Countries

Japan

Contacts

Public ContactKiyohiko Sato

Japanese Association for Acute Medicine Secretariat

editorial-jaam@umin.net+81-3-5840-9870

Outcome results