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Trials / Withdrawn

WithdrawnNCT03401125

Risk Factors for Allo-immunization in Sickle Cell Disease

Retrospective Study of the Risk Factors for Allo-immunization in Sickle Cell Disease

Status
Withdrawn
Phase
Study type
Observational
Enrollment
0 (actual)
Sponsor
Hanane EL KENZ · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Sickle cell patients have a high prevalence of alloimmunization. This high rate of alloimmunization can be partially explained by the existence of an antigenic difference between the predominantly Caucasian donor population and the sickle cell patients of African origin. Genetic and environmental risk factors have also been described. The main risk factors that have been shown in retrospective or cross-sectional studies are some HLA alleles, the age of the patient, the number of leukocyte-depleted erythrocyte concentrates (CED) transfused, the number of transfusion episodes, the age of the CEDs, the existence of an inflammatory event at the time of transfusion and the presence of anti-erythrocyte autoantibodies.There is also evidence of an impaired TH response but the underlying immunological mechanism is not fully understood. The aim of this study is to study the prevalence and the risk factors for anti-erythrocyte alloimmunization in pediatric and adult patients with Sickle Cell Disease (with a SS genotype) who are being followed at Queen Fabiola University Children's Hospital (HUDERF) and at the CHU Brugmann Hospital. The identification of risk factors would allow the investigators to improve, or at least adapt, their transfusion policy to certain clinical or immuno-haematological situations.

Conditions

Interventions

TypeNameDescription
OTHERMedical file data collectionThe information described in the 'outcome measures' section will be collected from the medical files of the patients.

Timeline

Start date
2018-02-01
Primary completion
2018-07-01
Completion
2018-07-01
First posted
2018-01-17
Last updated
2018-07-26

Locations

2 sites across 1 country: Belgium

Source: ClinicalTrials.gov record NCT03401125. Inclusion in this directory is not an endorsement.