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Analysis of Risk Factors for Coagulation Dysfunction in Patients with Traumatic Brain Injury

Analysis of Risk Factors for Coagulation Dysfunction in Patients with Traumatic Brain Injury

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109108
Enrollment
Unknown
Registered
2025-09-11
Start date
2025-09-22
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

Traumatic Brain Injury

Interventions

TIC Group:None
non-TIC Group:None

Sponsors

The Second Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, first time admitted to the ICU; 2. Diagnosed with TBI based on clinical manifestations and imaging examinations (such as CT or MRI), with a Head Abbreviated Injury Scale (AIS) score >= 3; 3. Laboratory results such as blood routine, coagulation function, liver and kidney function within 24 hours after admission.

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating women; 2. History of bleeding disorders; 3. Long-term, regular use of anticoagulants prior to injury; 4. Admission to this medical institution more than 24 hours after injury; 5. ICU hospitalization duration less than 24 hours; 6. Incomplete data: missing key information in medical records.

Design outcomes

Primary

MeasureTime frame
The occurrence of coagulation dysfunction;

Secondary

MeasureTime frame
Died during hospitalization;ICU hospitalization duration;Total hospitalization time;

Countries

China

Contacts

Public ContactTong Fei

The Second Hospital of Hebei Medical University

tongfei168@163.com+86 158 0321 0603

Outcome results

None listed

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