Actively Recruiting

All Genders
NCT03934112

Impact of Transfusional Practice on the Morbidity and Mortality of Patients in Intensive Care Unit

Led by Centre Hospitalier Universitaire de Besancon · Updated on 2024-09-19

150000

Participants Needed

1

Research Sites

360 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will allow correlating transfusion monitoring and patients' prognostic according to the chosen outcome criteria. These data could thus represent a basis for transfusion recommendations, except for intensive care and vital emergencies. It will also bring information about the actual transfusion monitoring in intensive care unit (ICU), in the period following the stay in the ICU and after hospital discharge.

CONDITIONS

Official Title

Impact of Transfusional Practice on the Morbidity and Mortality of Patients in Intensive Care Unit

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient admitted to medical and surgical resuscitation units of Besanon and Dijon university hospitals, all causes considered
  • Patient admitted between 1st January 2012 to 31st December 2017
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

CHU de Besançon

Besançon, France

Actively Recruiting

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Research Team

M

Maxime Desmarets, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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