NCT Number: NCT03313583
French One Day Survey in 2011 - Knowing Our Population of Labile Blood Products Recipients
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.
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Notify MeKey information
Conditions
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Transfusion with at least one blood product on the day of the study.
Exclusion criteria
- None
Treatment and study plan
Primary outcomes
-
Number of red blood cell concentrates received
Time frame: 1 day (cross sectional)
transversal study
-
Number of platelet concentrates recevied
Time frame: 1 day (cross sectional)
transversal study
-
Number of plasma units received
Time frame: 1 day (cross sectional)
transversal study
Sponsors and collaborators
Lead sponsor
Etablissement Français du Sang
Other
Collaborators
- Assistance Publique Hopitaux De Marseille
- Centre Hospitalier Universitaire de Besancon
- Centre Hospitalier Universitaire de Nice
- Région Nord-Pas de Calais, France
Registry information
Official study title
French Transfusion Recipients Cross Sectional Study : Get to Know the Transfusion Recipients Population
Acronym: PopReceveur
Important dates
- Study start
- 2011
- Primary completion
- 2011
- Study completion
- 2011
- First posted
- Oct 18, 2017
- Registry last updated
- Oct 18, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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