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ICU Cell Saver to Reduce Blood Transfusions in Cardiac

Routinely Use of CardioPAT Cell Saver in Cardiac Surgery: A Prospective Randomized Study Focused on Allogenic Blood Transfusion and Clinical Outcome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00950547
Enrollment
350
Registered
2009-07-31
Start date
2009-08-31
Completion date
2010-01-31
Last updated
2010-01-05

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

Conditions

Blood Transfusion, Cardiac Surgery

Keywords

Blood Transfusion, Cell Saver, Cardiac Surgery, Evaluate the efficacy of cell salvage CardioPAT routinely used in cardiac surgery in reducing blood transfusions.

Brief summary

PURPOSE: Autotransfusion devices may be employed in cardiac surgery to decrease allogenic blood requirements. Limitations of previous trials include the use of cell saver systems in selected high risk patients only or the lack of blood transfusion-sparing strategies. The aim of this prospective randomized study is to evaluate the efficacy of cell salvage CardioPAT routinely used in cardiac surgery. METHODS: The investigators will randomize 350 patients in two groups: group 1 receives a CardioPAT cell saver device (175 patients), group 2 doesn't receive any cell saver device. The incidence of allogenic blood transfusion and clinical outcome in both groups are evaluated.

Interventions

DEVICECARDIOPAT

Cell Saver System at bedside for ICU stay

DEVICETraditional Chest Drains

Chest drains as usual with no possibility to reinfuse lost blood

Sponsors

Cardiochirurgia E.H.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All patients presenting for cardiac Surgery

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frame
Number of Transfusions per patient10 days after surgery

Secondary

MeasureTime frame
Mortality30 days after surgery

Countries

Italy

Outcome results

None listed

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