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Clinical trial of transfusion efficacy influenced by red blood cell storage lesion

Efficacy of transfusion influenced by red blood cell storage lesion: a randomised, double-blind, prospective clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002683
Enrollment
Unknown
Registered
2012-04-04
Start date
2011-05-25
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

patients who need transfusion

Interventions

1:red blood cell storage for 1 week
2:red blood cell storage for 2 weeks
3:red blood cell storage for 3 weeks

Sponsors

Xinqiao Hospital, Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 89 Years

Inclusion criteria

Inclusion criteria: Patients undergoing surgery with transfusion needs;patients suffering Hematologic Malignancies with transfusion needs; patients with transfusion needs in department of Oncology; without sex and age restriction; voluntary to participate and signed the informed consent.

Exclusion criteria

Exclusion criteria: Patients transfused other blood components within 24 hours after red blood cell transfusion; administration stimulant medicines such as hormone within 24 hours after transfusion; bleeding patients (hemoglobin less than 30 mg/L); patients didn't sign informed consent; data only be collected once in patients need multiple transfusions.

Design outcomes

Primary

MeasureTime frame
Hematocrit;hemoglobin;pH;pCO2;pO2;SO2;—

Countries

China

Contacts

Public ContactZhongjun Li
lizhungjun@yahoo.com.cn+86 023 68755319

Outcome results

None listed

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