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Randomized Trial of a Liberal Versus a Restrictive Transfusion Strategy in Elderly Cardiac Surgery Patients

Evaluation of a Liberal Versus Restrictive Blood Transfusion Strategy in Elderly Patients Following Coronary Bypass or Aortic Valve Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00318227
Enrollment
73
Registered
2006-04-26
Start date
2004-06-21
Completion date
2010-02-23
Last updated
2017-08-28

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

Conditions

Anemia, Coronary Artery Bypass Surgery

Keywords

Postoperative care, Cardiac Surgery, Blood Transfusion

Brief summary

The purpose of this study is to determine whether a less restrictive strategy of red blood cell transfusion in elderly patients following coronary bypass surgery results in enhanced postoperative recovery as determined by quality of life assessment, exercise tolerance and clinical outcomes. Two postoperative transfusion strategies: 1. Liberal - transfused when Hgb is \<100g/L 2. Restrictive - transfused when Hgb is \<70g/L

Interventions

PROCEDUREBlood Transfusion

Blood transfusion will be administered when the transfusion trigger is met.

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
70 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Patients \>=70 years of age undergoing non-emergency coronary artery bypass surgery * Initial postoperative hemoglobin level 70-90g/L

Exclusion criteria

* Patients who are unable to provide informed consent in English * Patients with preoperative hemoglobin concentrations \<100g/L * Patients who require emergency re-operation * Patients with intraoperative or postoperative bleeding diathesis * Patients with postoperative clinical instability (eg. low output state) * Patients in whom insertion of an intra-aortic balloon pump is required

Design outcomes

Primary

MeasureTime frame
Distance walked during 6 minute walk test at 5 weeks postop5 weeks

Secondary

MeasureTime frame
renal failure, hospital length of stay, Quality of Life questionnaireduring hospital stay

Countries

Canada

Outcome results

None listed

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