Study to Understand the Genetic Risk of Developing an Immune Response After Blood Transfusions Among Individuals With Sickle Cell Disease
Part of paid clinical trials in Bethesda, Maryland.
- Sponsor
- National Human Genome Research Institute (NHGRI)
- Study ID
- NCT06944067
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 2 Years - 99 Years
- Healthy Volunteers
- Not accepted
Study Details
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.
Key Dates
- Start date
- Jun 24, 2025
- Status verified
- May 2026
- Primary completion
- Apr 10, 2030
- Completion
- Apr 10, 2030
Study Design
- Enrollment
- 50 participants (estimated)
Arms
- Arm: Alloimmune non-respondersIndividuals with sickle cell disease who have received blood transfusions but never had an alloimmune response to transfusion.
- Arm: Alloimmune respondersIndividuals with sickle cell disease who have a history of an alloimmune response when receiving blood transfusions.
Primary Outcome Measure
Completion of analysis of previously identified risk loci to determine the relationship between genome structure and expression. [ Time Frame: 5 years ]
Central Contacts
- Emilyn C Banfield(240) 328-0965
- Neil A Hanchard, M.D.(301) 594-2151
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| National Institutes of Health Clinical Center | Bethesda | Maryland | 20892 |
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