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The clinical effect of length of pre-transfusion storage of blood

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN06273643
Enrollment
20
Registered
2003-09-12
Start date
2000-08-31
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

Anaemia Haematological Disorders Other anaemias

Interventions

Stable patients requiring blood transfusions for anaemia more often than every 6 weeks will be recruited. They will be randomised to receive two transfusions of four units of "fresh" blood (less than

Sponsors

Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients 18 and over with a haematological disorder requiring regular red cell transfusion (eg myelodysplastic syndrome, aplastic anaemia, etc) 2. Able to give informed consent 3. Serum creatinine <200 umol/l within past 2 months

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
48-hour post transfusion haemoglobin (Hb) increment.

Secondary

MeasureTime frame
1. Changes in red cell 2,3-DPG concentration and Hb-oxygen affinity (P50) 2. Subsequent changes in Hb at 14 days and before next transfusion 3. Changes in patients' quality of life (QOL) as measured by SF-36 health survey and a visual analogue scale

Countries

United Kingdom

Outcome results

None listed

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