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Preventive extended red blood cell antigen matching: when and how?

Preventive extended red blood cell antigen matching: when and how? - Match study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON31145
Enrollment
1120
Registered
2007-09-25
Start date
2008-06-27
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Aandoeningen die als ondersteuning van de therapie/ingreep bloedtransfusie vereisen No specific disease

Interventions

Standard ABO-D compatible versus extended (C,c,E,e,K,Fya,Jka and S) compatible red blood cell products. Both have equal standard product-specifications

Sponsors

Sanquin Bloedbank
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: The general transfusion population >18 years requiring an elective RBC transfusion

Exclusion criteria

Exclusion criteria: Patients younger than 18 years Patients with an a priori indication for matched transfusions (congenital hemolytic anemia*s, immune hemolytic anaemia, females of (pre-) childbearing age) Patients with a positive DAT Patients who, based on the local pre-operative blood-ordering list, require more than 4 RBC units during surgery. Incapacitated subjects or patients who cannot understand the information.

Design outcomes

Primary

MeasureTime frame
Incidence of alloimmunization in transfusion patients through preventive donor matching for clinically relevant antibodies compared to standard matching in patients stratified for high and random risk alloimmunization

Secondary

MeasureTime frame
1. Cost-analysis for current serologic screen and match strategy compared to preventive matching strategy in the 2 strata of patients 2. Investigate transfusion and/or other medical treatment delay in case of RBC alloimmunization 3. Obtain data on clinical and genetic factors associated with RBC alloimmunization

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)