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The Impact of Red Packed Cells Transfusion on the Main Biological Markers to Determine the Etiology of Anemias

The Impact of Red Packed Cells Transfusion on the Main Biological Markers to Determine the Etiology of Anemias

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01409967
Acronym
BÉA/T
Enrollment
40
Registered
2011-08-04
Start date
2011-05-31
Completion date
2013-08-31
Last updated
2013-08-26

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

Conditions

Anemia

Keywords

Anemia, Transfusion, Biological markers

Brief summary

The aim of this work is to study the changes of key assays useful for the understanding of anemia mechanism before and after red packed cells transfusion: iron status, vitamin assays, hemolysis markers.

Detailed description

The aim of this work is to study the changes of key assays useful for the understanding of anemia mechanism before and after red packed cells transfusion: iron status, vitamin assays, hemolysis markers. The patient selection criteria are: * age \> or = 18 years * No history of transfusion \> or = 2 years * Anemia (any etiology known or assumed) * Decision of red packed cells transfusion for the current episode * Transfusion performed at BEAUJON Hospital * Agreement of patient for the study Number of subjects required: 100 patients Study duration and duration of participation for each patient: * duration of the study: 1 year * for each patient the participation to the study began at baseline after the decision of transfusion and stopped at the second sample ie at least 72 hours after the transfusion of red blood cells. The maximum contribution for one patient is 5 days. Methodology: It is a prospective non interventional monocentric (BEAUJON Hospital) study. Two blood tests will be performed; one before transfusion and the other from 48 to 72 hours after red packed cells transfusion. The following parameters will be measured before and after red packed cells transfusion: Complete blood count (CBC) with reticulocyte count; complete iron status (ferritin, serum iron, transferrin, transferrin saturation), soluble transferrin receptor; serum and intraerythrocytic folate levels, vitamin B12; lactate dehydrogenase (LDH), bilirubin (total and free), haptoglobin, orosomucoid, direct coombs test; creatinine; CRP. The aim of this work is to study the changes of key assays useful for the understanding of anemia mechanism before and after red packed cells transfusion: iron status, vitamin assays, hemolysis markers.

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> or = 18 years * No history of transfusion \> or = 2 years * Anemia (any etiology known or assumed) * Decision of red packed cells transfusion for the current episode * Transfusion performed at BEAUJON Hospital * Agreement of patient for the study

Exclusion criteria

* Patient who received between the 2 samples, a treatment which can modify the parameters evaluated (iron, vitamin)

Design outcomes

Primary

MeasureTime frame
anemia72 hours

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026