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Clinical research on administration of ubiquitin-removed stored red blood cell attenuating transfusion immunosuppressive effects

Clinical research on administration of ubiquitin-removed stored red blood cell attenuating transfusion immunosuppressive effects

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037576
Enrollment
Unknown
Registered
2020-08-28
Start date
2020-11-01
Completion date
Unknown
Last updated
2020-11-02

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

Conditions

Transfusion of red blood cell

Interventions

Group 1:Transfusion of ubiquitin-removed stored red blood cell
Group 2:Transfusion of not ubiquitin-removed stored red blood cell

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. Adult patients undergoing total hip replacement who experiences excessive bleeding during intraoperative period and receive red blood cell transfusion, or hemoglobin<8g/dl, or patients who has anemia during perioperative period; 3. Adult patients undergoing cardiac surgery who experiences excessive bleeding during intraoperative period and receive red blood cell transfusion, or hemoglobin<7.5g/dl, or patients who has anemia during perioperative period; 4. Adult patients undergoing liver transplantation surgery who experiences excessive bleeding during intraoperative period and receive red blood cell transfusion, or hemoglobin<8g/dl, or patients who has anemia during perioperative period; 5. Adult patients undergoing acute gastrointestinal bleeding and receive red blood cell transfusion, or hemoglobin<7g/dl, or according to the patients cardiopulmonary, metabolism, oxygen consumption and hemodynamic conditions; 6. Adult patients undergoing tumor resection surgery who experiences excessive bleeding during intraoperative period and receive red blood cell transfusion, or hemoglobin<7g/dl, or patients who has anemia during perioperative period 7. Adult patients who has hematological malignanciessuch as: lymphoma, leukemia, myelodysplastic syndromesaplastic anemiahemoglobin<7g/dl, or according to the patients cardiopulmonary, metabolism, oxygen consumption and hemodynamic conditions; 8. Patients with complete clinical examination, laboratory examination, medical record and medical history.

Exclusion criteria

Exclusion criteria: 1. Psychiatric disorders; 2. Patients who dont have complete clinical data; 3. Patients who undergoing surgery or gastrointestinal bleeding, hematological malignancies should be excluded, and no immunomodulatory drugs be used during transfusion and examination; 4. Patients who have hematological malignancies should be in their intermission of chemotherapy, and no immunomodulatory drugs be used during transfusion and examination.

Design outcomes

Primary

MeasureTime frame
Adverse Event after transfusion;immunocyte function;

Secondary

MeasureTime frame
Hospital stay;

Countries

China

Contacts

Public ContactRong Xia

Department of Blood Transfusion, Huashan Hospital, Fudan University

xiarongcn@126.com+86 021-52888329

Outcome results

None listed

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