Observational Study to Determine Red Blood Cell Alloimmunization Risk Etiology in Patients With Sickle Cell Disease

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The purpose of this research study is to look at genes and determine how they interact with each other to find changes that could explain why some people's immune systems may respond to blood transfusions. This response is called an alloimmune response. We strongly believe that when someone has an alloimmune response, it is caused by changes in their genes. We plan to compare changes in the genes of individuals that develop red blood cell alloimmunization after blood transfusions with those that do not develop alloimmunization. This may help us to create more targeted therapeutic interventions, which may improve the health of alloimmune responders.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 99
Healthy Volunteers: f
View:

⁃ To be eligible to participate in this study, an individual must meet all of the following criteria:

⁃ 1\. Individual (\> 2 years of age) with confirmed SCD diagnosis who meets at least one of the following conditions:

• History of greater than ten administered transfusions or 20 transfusion units (where known)

• History of one or more antibody screens

• Known candidate variant genotype

Locations
United States
Maryland
National Institutes of Health Clinical Center
RECRUITING
Bethesda
Contact Information
Primary
Emilyn C Banfield
SCDtransfusionstudy@mail.nih.gov
(240) 328-0965
Backup
Neil A Hanchard, M.D.
neil.hanchard@nih.gov
(301) 594-2151
Time Frame
Start Date: 2025-06-24
Estimated Completion Date: 2030-04-10
Participants
Target number of participants: 50
Treatments
Alloimmune non-responders
Individuals with sickle cell disease who have received blood transfusions but never had an alloimmune response to transfusion.
Alloimmune responders
Individuals with sickle cell disease who have a history of an alloimmune response when receiving blood transfusions.
Sponsors
Leads: National Human Genome Research Institute (NHGRI)

This content was sourced from clinicaltrials.gov