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NCT03313583 Clinical Trial

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

Trauma Clinical Trial

— PopReceveur  

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03313583
Other study ID # EFS/2011/PopReceveur
Secondary ID
Status Completed
Phase N/A
First received September 29, 2017
Last updated October 17, 2017
Start date November 1, 2011
Est. completion date December 1, 2011

Study information
Verified date October 2017
Source Etablissement Français du Sang
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 4720
Est. completion date December 1, 2011
Est. primary completion date November 1, 2011
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

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

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Transfusion of blood products

Locations
Country Name City State
n/a

Sponsors (5)
Lead Sponsor Collaborator
Etablissement Français du Sang Assistance Publique Hopitaux De Marseille, Centre Hospitalier Universitaire de Besancon, Centre Hospitalier Universitaire de Nice, Région Nord-Pas de Calais, France

References & Publications (1)

Fillet AM, Desmarets M, Assari S, Quaranta JF, François A, Pugin A, Schuhmacher A, Lassale B, Monnet E, Cabre P, Legrand D, Binda D, Djoudi R. Blood products use in France: a nationwide cross-sectional survey. Transfusion. 2016 Dec;56(12):3033-3041. doi: — View Citation

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