Skip to content

Development and validation of a prediction model of progressive hemorrhagic injury after traumatic brain injury

Development and validation of a prediction model of progressive hemorrhagic injury after traumatic brain injury

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100046571
Enrollment
Unknown
Registered
2021-05-22
Start date
2021-05-21
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

traumatic brain injury

Interventions

PHI group:NA
Non-PHI group:NA

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged > 18 years; 2. There is a clear history of head trauma, and the presence of brain contusion is confirmed by head CT scan; 3. It is not accompanied by serious damage to other parts of the brain, and the abbreviated injury scale (AIS) score of other parts outside the skull is <= 3 points; 4. The first CT scan of the head is within 6 hours after the injury, and at least one CT scan is performed within 72 hours after admission.

Exclusion criteria

Exclusion criteria: 1. The indications for craniotomy on admission are clearly needed for emergency craniotomy; 2. Take anticoagulant and antiplatelet drugs (warfarin, aspirin, clopidogrel, etc.); 3. Combined with severe liver, spleen, kidney and other organ damage and severe hemorrhagic shock; 4. Open brain injury (such as gunshot wound, sword wound, etc.); 5. Pre-existing diseases such as renal insufficiency and abnormal parathyroid function; intake of drugs or diseases that affect calcium metabolism (such as abnormal parathyroid function, malignant tumors, massive blood transfusion, etc.); 6. Known past brain diseases (traumatic or non-traumatic) accompanied by permanent neurological defects; 7. Known history of autoimmune diseases; 8. Acute or chronic infectious diseases; 9. Pregnancy.

Design outcomes

Primary

MeasureTime frame
Demographic data;Clinical data at admission;Imaging parameters at admission;Laboratory indicators at the time of admission;

Countries

China

Contacts

Public ContactZhuge Qichuan

The First Affiliated Hospital of Wenzhou Medical University

1146584817@qq.com+86 15397430178

Outcome results

None listed

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