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Determination of Red Cell Survival in Sickle Cell Disease and Other Hemoglobinopathies Using Biotin Labeling

We study red blood cell lifespan in sickle cell disease.

Recruiting
18 years and older
All
Phase 0

Sickle cell disease (SCD) is a blood disorder where red blood cells (RBCs) die too early, causing a shortage of healthy cells. This study wants to find out how long RBCs last in people with SCD and other blood disorders, especially before and after treatment or a bone marrow transplant. Participants must be 18 or older, with SCD or a similar disorder, and those who had a transplant. In this study, about 7 tablespoons of blood will be taken and mixed with biotin (a type of vitamin) that sticks to RBCs. The next day, these biotin-labeled RBCs are returned to the participant. Participants come back for regular visits to have smaller blood samples taken to see how many biotin-labeled RBCs are still there. This may happen every 2-4 weeks for up to 20 weeks.

  • Duration: Up to 20 weeks, with regular visits.
  • Eligibility: Adults 18+ with SCD or related disorders, post-transplant patients.
  • Risks: Exclusion if allergic to biotin or recent blood transfusions.
Study details
    Sickle Cell Disease
    Thalassemia
    Hemoglobinopathy

NCT06313398

National Heart, Lung, and Blood Institute (NHLBI)

17 October 2026

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