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OpenTrials
Completed

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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Key information

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

Transfusion of blood products

Procedure

Primary outcomes

  1. Number of red blood cell concentrates received

    Time frame: 1 day (cross sectional)

    transversal study

  2. Number of platelet concentrates recevied

    Time frame: 1 day (cross sectional)

    transversal study

  3. 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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