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Blood transfusion and Clinical outcomes in patients with severe trauma: a multicenter prospective cohort study

Blood transfusion and Clinical outcomes in patients with severe trauma: a multicenter prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019688
Enrollment
Unknown
Registered
2018-11-23
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

Severe trauma

Interventions

Group 1:red blood cell transfusion
Group 2:massive transfusion
Group 3:non-transfusion

Sponsors

The First Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged = 18 years; 2. Admission within 4 hours after injury; 3. Injury Severity Score = 16; 4. Patients with informed consent and signature of informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. High variability of clinical outcomes due to cases transferred to other medical institutions after treatment but not recorded or controlled by other medical institutions; 3. Coagulation factor deficiency disease, thrombocytopenia; 4. History of severe heart, lung, liver, kidney, tumor and other important organ diseases; 5. Lung infection, urinary tract infection, wound infection at admission; 6. May die within 1 hour after admission; 7. Burn surface area = 20% or suspicious inhalation injury; 8. Participated in other clinical studies.

Design outcomes

Primary

MeasureTime frame
morality;

Secondary

MeasureTime frame
complication;length of stay;ICU length of stay;red blood cell transfusion volume;plasma transfusion volume;platelet transfusion volume;cryoprecipitation transfusion volume;

Countries

China

Contacts

Public ContactLe Aiping

The First Affiliated Hospital of Nanchang University

leaiping@126.com+86 0791-88692263

Outcome results

None listed

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