French One Day Survey in 2011 - Knowing Our Population of Labile Blood Products Recipients

French Transfusion Recipients Cross Sectional Study : Get to Know the Transfusion Recipients Population

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03313583

Acronym

PopReceveur

Enrollment

4720

Registered

2017-10-18

Start date

2011-11-01

Completion date

2011-12-01

Last updated

2017-10-18

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

Conditions

Blood Product Transfusion for All Conditions, Hematologic Diseases, Surgical Blood Loss, Trauma

Brief summary

Describe the epidemiologic profile and clinical context of transfusion recipients in France. Describe the clinical context of transfusion. Describe the characteristics of the transfusion prescriptions, the use of blood products and the main indications for transfusion. Describe transfusion practice according the type of hospital stay.

Interventions

PROCEDURETransfusion of blood products

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

• Transfusion with at least one blood product on the day of the study.

Exclusion criteria

* None

Design outcomes

Primary

Measure	Time frame	Description
Number of platelet concentrates recevied	1 day (cross sectional)	transversal study
Number of plasma units received	1 day (cross sectional)	transversal study
Number of red blood cell concentrates received	1 day (cross sectional)	transversal study

Outcome results

None listed

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