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Clinical Trials/NL-OMON36804
NL-OMON36804
Completed
Not Applicable

The Effects of Transfusion of Red blood cells In Sepsis - TETRIS, Transfusion in Sepsis

Academisch Medisch Centrum0 sites100 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sepsis + blood poisoning
Sponsor
Academisch Medisch Centrum
Enrollment
100
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients who will receive their first erythrocyte transfusion on the ICU to correct for anemia

Exclusion Criteria

  • \- Patients who have not given informed consent
  • \- Patients who pose difficulties in securing blood products (e.g. rare blood groups)
  • \- Patients who are actively bleeding or are suspected for active bleeding (when a transfusion is given with the intention to treat bleeding according to the treating physician)
  • \- Patients who receive more than 1 unit of red blood cells in the transfusion episode
  • \- Patients who need a blood transfusion when there\*s no fresh blood available

Outcomes

Primary Outcomes

Not specified

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