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Clinical Trials/NCT04101240
NCT04101240
Unknown
Not Applicable

Impact of Perioperative Anemia and Red Blood Cells Transfusion on Post-operative Complications After Oncological Surgery

University Hospital, Brest1 site in 1 country300 target enrollmentFebruary 7, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anemia
Sponsor
University Hospital, Brest
Enrollment
300
Locations
1
Primary Endpoint
Number of mortality or any respiratory, cardiac, renal, thromboembolic, infectious and/or hemorrhagic post operative complications
Last Updated
6 years ago

Overview

Brief Summary

Oncologic patients experience anemia and anemia is associated with poor prognosis. Transfusion is associated with adverse events, and equipoise remains on the optimal transfusion strategy in oncologic patients in surgical setting. The primary objective of this study is to determine the impact of anemia and red blood cells (RBC) transfusion on post-operative complications and mortality.

Detailed Description

Between 36 and 75% of oncologic patients experience anemia and anemia is associated with poor prognosis. Up to 40% of surgical oncologic patients receive red blood cells (RBC). However, transfusion is associated with adverse events, and equipoise remains on the optimal transfusion strategy in oncologic patients in surgical setting. The primary objective of this study is to determine the impact of anemia and red blood cells (RBC) transfusion on post-operative complications and mortality. This is a retrospective, single center study. All adults admitted to the intensive care unit (ICU) after oncologic surgery within the study period are eligible.

Registry
clinicaltrials.gov
Start Date
February 7, 2019
End Date
November 30, 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Surgery for cancer
  • Admission to intensive care

Exclusion Criteria

  • no consent

Outcomes

Primary Outcomes

Number of mortality or any respiratory, cardiac, renal, thromboembolic, infectious and/or hemorrhagic post operative complications

Time Frame: 30 DAYS (hospital discharge)

mortality or any respiratory, cardiac, renal, thromboembolic, infectious and/or hemorrhagic post operative complications

Study Sites (1)

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