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Bone-related problems represent the principal unmet medical need in Gaucher disease (GD). 75% of GD type 1 patients develop skeletal complications, including bone remodeling defects, osteopenia, osteoporosis, marrow infiltration, avascular necrosis, and osteolysis. However, the underlying cellular/molecular basis of bone involvement and related complications in GD are not fully known. Neither are there any bone-specific markers associated with individual bone pathology. Early diagnosis of bone disease is the key issue for planning individual therapy to prevent and reverse bone disease in GD.
Full description
This clinical observational study is designed to identify specific biomarkers for bone involvement in patients with GD1 with decreased bone density and/or bone structural abnormalities
Aims:
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Inclusion criteria
To be enrolled in this study the subject must meet the following criteria
Subject is greater than 16 years old but not older than 90 years
Signed Informed Consent/Assent
Subject is able and willing to sign informed consent or assent
If the subject has GD1, the must have a confirmed diagnosis of Gaucher disease by
Exclusion criteria
40 participants in 4 patient groups
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Central trial contact
Margarita Ivanova, PhD; Jacqueline Fikry
Data sourced from clinicaltrials.gov
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