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Clinical blood transfusion and prognosis in patients with major burn: a multicenter prospective cohort study

Clinical blood transfusion and prognosis in patients with major burn: a multicenter prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019689
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

major burn

Interventions

massive plasma transfusion group:plasma transfuion =2000mL
non-plasma transfuion group:plasma transfuion < 2000mL
non-transfusion group:No plasma transfusion

Sponsors

The First Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Aged at least 18 years old; (2) admitted to the hospital within 4 hours after the burn; (3) The burn area is =30%; (4) Patients who gave informed consent and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) pregnant or lactating women; (2) Transferred by other medical institutions after treatment, but the case data provided by other medical institutions cannot record or control the quality, resulting in high variability of clinical results; (3) coagulation factor deficiency, thrombocytopenia; (4) a history of serious organ diseases such as heart, lung, liver, kidney and tumor; (5) Pulmonary infection, urinary tract infection, and wound infection have occurred at the time of admission; (6) may die within 1 hour after admission; (7) Participated in other clinical studies.

Design outcomes

Primary

MeasureTime frame
24 h mortality;in-hospital mortality;30 d mortality;

Secondary

MeasureTime frame
complications;length of stay;ICU length of stay;

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