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Anemia and Red Blood Cells Transfusion in Oncological Surgery

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04101240
Acronym
IMPACT
Enrollment
300
Registered
2019-09-24
Start date
2019-02-07
Completion date
2019-11-30
Last updated
2019-09-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anemia, Oncology, Surgery

Keywords

red blood cells transfusion

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.

Interventions

None listed

Sponsors

University Hospital, Brest
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Surgery for cancer * Admission to intensive care

Exclusion criteria

* no consent

Design outcomes

Primary

MeasureTime frameDescription
Number of mortality or any respiratory, cardiac, renal, thromboembolic, infectious and/or hemorrhagic post operative complications30 DAYS (hospital discharge)mortality or any respiratory, cardiac, renal, thromboembolic, infectious and/or hemorrhagic post operative complications

Countries

France

Contacts

Primary ContactCécile AUBRON, PU PH
cecile.aubron@chu-brest.fr+33298347181

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026