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Correlation study between the changes of coagulation function and clinical prognosis in patients with severe trauma

Correlation study between the changes of coagulation function and clinical prognosis in patients with severe trauma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055311
Enrollment
Unknown
Registered
2022-01-06
Start date
2022-01-01
Completion date
Unknown
Last updated
2023-01-23

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

Conditions

severe trauma

Interventions

case series:Nil

Sponsors

The Second Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 and above; 2. Patients who are confirmed to be severely traumatized (GCS110 times/min or TI>10 points) or those who are considered to be at risk of serious bleeding; 3. Those who come to the hospital within 3 hours of being injured and enter the emergency resuscitation unit.

Exclusion criteria

Exclusion criteria: 1. Previous history of abnormal coagulation disorders or long-term oral anticoagulant and antiplatelet drugs; 2. History of long-term alcoholism, malignant tumor, organ dysfunction, venous thromboembolism, etc.; 3. Those with contraindications to the use of tranexamic acid: (1) Those who are allergic to tranexamic acid; (2) Those who are using thrombin; 4. Cardiopulmonary arrest due to trauma before admission.

Design outcomes

Primary

MeasureTime frame
Mortality within four weeks after injury;

Secondary

MeasureTime frame
Changes of coagulation function;

Countries

China

Contacts

Public ContactLiu Lijun

The Second Affiliated Hospital of Soochow University

lijunliusz@sina.com+86 13962192756

Outcome results

None listed

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