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Haemorrhage From Severe Neck and Facial Injuries - Characteristics, Management and Outcomes

Haemorrhage From Severe Neck and Facial Injuries - Characteristics, Management and Outcomes

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07204405
Enrollment
15000
Registered
2025-10-02
Start date
2015-01-01
Completion date
2025-06-01
Last updated
2025-10-02

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

Conditions

Facial Bones Fracture, Neck Injuries, Trauma (Including Fractures)

Keywords

Facial injury, Neck injury, Trauma, Bleeding

Brief summary

This is a descriptive observational study of trauma patients admitted to the Trauma Unit at the Karolinska University Hospital Solna, Stockholm, Sweden. Data will be collected from the Karolinska Trauma Registry for all patients from 2015 to 2024. A more detailed dataset will be extracted from the Trauma Registry for all patients with serious facial or neck injuries. For those patients, data will also manually be extracted from their clinical records.

Detailed description

Data will be collected from the Karolinska Trauma Registry for all patients from 2015 to 2024. A more detailed dataset will be extracted from the Trauma Registry for all patients with an Abbreviated Injury Scale (AIS) severity score of ≥ 3 for facial or neck injuries. Data will include demographics, injury mechanism, injury type, physiology, treatment and outcome. For those patients with a severe facial or neck injury, data will also manually be extracted from their clinical records regarding prehospital details, initial physiology, injury type, treatment and bleeding.

Interventions

None listed

Sponsors

Karolinska Institutet
CollaboratorOTHER
Karolinska University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients included in the Karolinska Trauma Registry

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Death from bleeding30 daysDeath from bleeding within 30 days.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026