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Low-Titer Group O Whole Blood for Emergency Transfusion in Non-Group O Patients: A Multicenter, Prospective Study

Clinical Study of Low-Titer O Whole Blood in Non-Type O Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109572
Enrollment
Unknown
Registered
2025-09-22
Start date
2025-09-22
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

Trauma bleeding and surgical bleeding

Interventions

LTOWB group:Transfusion was initiated in accordance with the transfusion indications outlined in WS/T 623—2018: Guidelines for the Use of Whole Blood and Blood Components. The initial transfusion cons
Component blood group:Red blood cells, plasma, and platelets were transfused in accordance with the transfusion indications specified in WS/T 623—2018: Guidelines for the Use of Whole Blood and Blood

Sponsors

The First Medical Center of the Chinese People's Liberation Army General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Adult patients: aged 18 to 70 years old (inclusive of 18 and 70 years old), regardless of gender, with blood types A, B, or AB and RhD positive. 2.Have received at least 2U of LTOWB or red blood cells. 3.Patients undergoing elective surgeries that require a large amount of blood reservation. 4.Traumatic bleeding patients who are expected to receive a large - volume blood transfusion. 5.Requirements for the type of surgery: patients planning to undergo liver surgery, orthopedic surgery. 6.Be capable of signing the informed consent form for the study.

Exclusion criteria

Exclusion criteria: 1.History of transfusion reactions or severe allergies. 2.Preoperative use of anticoagulants, antiplatelet agents, or other drugs that may affect coagulation function. 3.Presence of red blood cell antibodies. 4.Combined immunodeficiency or autoimmune diseases. 5.Combined end-stage liver disease or renal failure. 6.Active infectious diseases or hematologic malignancies. 7.Subject or family members refuse to participate in the study. 8. Participation in any other clinical trial within 4 weeks prior to the start of this study.

Design outcomes

Primary

MeasureTime frame
Transfusion reaction;

Secondary

MeasureTime frame
Red blood cell transfusion volume;Total blood transfusion volume;Blood loss;TEG;Coagulation function;Blood routine;Biochemistry;Direct antiglobulin test;Blood type;Irregular antibody;Blood transfusion time;Intensive Care Unit Time;Hospitalization period;

Countries

China

Contacts

Public ContactYu yang

Department of Transfusion Medicine, The First Medical Center of Chinese PLA General Hospital

yuyangpla301@163.com+86 10 6693 7132

Outcome results

None listed

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