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Does routine peri-operative continuous cell salvage in cardiac surgery reduce exposure to allogeneic blood? A randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17615029
Enrollment
206
Registered
2005-05-24
Start date
2005-05-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Blood transfusion following cardiac surgery Surgery Cardiac surgery

Interventions

Patients will be randomised to either the cell saver or control group. A Continuous Auto-Transfusion System (CATS, Fresenius Hemocare) cell saver will be used intra- and post-operatively with the aim

Sponsors

Papworth Hospital NHS Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients for non-emergency first-time Coronary Artery Bypass Grafting (CABG) with planned use of cardiopulmonary bypass, and patients for valve repair or replacement, or combined CABG and valve procedure.

Exclusion criteria

Exclusion criteria: 1. Refusal to receive blood or blood products 2. Previous cardiac or thoracic surgery 3. Having an unacceptable risk, as per investigator judgement 4. Known serious coagulation disorders 5. Known blood disorder (thalassemia, chronic anaemia, lymphoproliferative disorder etc.) 6. Any contra-indication to antifibrinolytics 7. The receipt of any investigational drug or participation in a device trial during the course of this trial 8. Where a specific request for cell salvage has been made by the surgeon

Design outcomes

Primary

MeasureTime frame
The proportion of patients exposed to allogeneic blood. All outcomes measured at 30 days post surgery.

Secondary

MeasureTime frame
1. The number of units of allogeneic red blood cells transfused during first-time cardiac surgery 2. The use of blood products such as fresh frozen plasma and platelet concentrates 3. Adverse events 4. Resource use and cost savings of using CATS in this specific group of patients All outcomes measured at 30 days post surgery.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026