- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03934112
Impact of Transfusional Practice on the Morbidity and Mortality of Patients in Intensive Care Unit (PATMORE)
Impact of Transfusional Practice on the Morbidity and Mortality of Patients in Intensive Care
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.
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion criteria:
- Patient admitted to medical and surgical resuscitation units of Besançon and Dijon university hospitals, all causes considered
- Patient admitted between 1st January 2012 to 31st December 2017
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Survival at 90 days after leaving ICU
Time Frame: Day 90
|
All-cause mortality 90 days after leaving ICU
|
Day 90
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- API/2016/72
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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