RH Genotype Matched RBC Transfusions
Recruiting now · Phase 1/Phase 2
Conditions studied: Sickle Cells Disease
In brief
To determine the feasibility and efficacy of matching donor red cells by RH genotype for a cohort of chronically transfused patients with SCD.
Key facts
- Study ID
- NCT04156893
- Run by
- Children's Hospital of Philadelphia
- People needed
- 35
- Starts
- 2020-01-30
- Expected to finish
- 2029-10-01
- Last updated by the study team
- 2026-04-27
Who can join
Age: 1 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects age >6 months
- Diagnosis of SCD, all genotypes
- Require a period of chronic red cell transfusion therapy
- Subject/parental/guardian permission (informed consent) and if appropriate, child assent
You may not qualify if…
- Rare RH genotype that would preclude identification of sufficient RBC units
- Antigen negative requirements due to alloimmunization that would preclude identification of sufficient RBC units
- Alloimmunized to D antigen
- Rh alloimmunized patients for whom providing RH genotype matched blood would expose the patient to an antigen that would not be consistent with standard of care and blood bank protocols
- Parents/guardians or subjects who, in the opinion of the Investigator, may be non-compliant with study schedules or procedures
Where it is running
- Children's Hospital of Philadelphia — Philadelphia, Pennsylvania, United States (enrolling)
Full record on ClinicalTrials.gov
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