Sickle Cell Disease Biofluid Chip Technology (SCD BioChip)
NCT02824471 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2025-08-21
Summary
'Sickle-shaped' anemia was first clinically described in the US in 1910, and the mutated heritable sickle hemoglobin molecule was identified in 1949. The pathophysiology of SCD is a consequence of abnormal polymerization of sickle hemoglobin (HbS) and its effects on red cell membrane properties, shape, and density, and subsequent critical changes in inflammatory cell and endothelial cell function. Our goal is to understand the impact of CMA abnormalities in SCD, by interrogating a number of recognized interactions in a range of clinical phenotypes.
To date, correlative studies in SCD, by us and others, have range between clinical reports, based on tests, interventions, and chart review of individuals or groups of individuals and, at the other extreme, identification of functional gene polymorphisms based on population studies. The investigators wish to augment these studies through a systematic examination of cellular membrane properties and activation status. Of hematologic disorders, SCD may be unusually susceptible to such an examination.
Conditions
Interventions
- OTHER
-
SCD Group
No Intervention. Use of discard blood/tissue
Sponsors & Collaborators
-
Case Western Reserve University
collaborator OTHER -
University Hospitals Cleveland Medical Center
lead OTHER
Principal Investigators
-
Amma Owusu-Ansah, MD · University Hospitals Cleveland Medical Center
Eligibility
- Min Age
- 12 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2014-10-31
- Primary Completion
- 2028-05-31
- Completion
- 2028-05-31
Countries
- United States
Study Locations
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