CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 60 enrolled
Drug / intervention
genetic analysesgenetic
Likely dose
Not stated in record
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Search/NCT02650219
NCT02650219N/ACompleted

Prevalence of Autoantibodies in the Gaucher Disease and the Role of CD1 Molecules in Immune Manifestations of This Disease

Hospital St. Joseph, Marseille, France·observational·Posted Jan 8, 2016·Updated Mar 23, 2016

In Brief

An observational study evaluating genetic analyses for Gaucher Disease. Completed, enrolled 60 participants across 11 sites.

Detailed Summary

Hypergammaglobulinaemia is frequently observed in type 1 Gaucher disease (GD1), being either polyclonal or monoclonal gammopathies. Polyclonal hypergammaglobulinemia may be related to the presence of autoantibodies. The clinical significance of such antibodies is questioned in Gaucher disease (GD), as some cases of immunologic thrombocytopenia and autoimmune hemolytic anemia have also been reported. Objectives: To evaluate the prevalence of autoantibodies and autoimmune diseases in GD1 patients, we conducted a multicenter national study. The investigators investigated whether there was a link between splenectomy, genotype, therapeutic options and the presence of these autoantibodies.They also investigated whether there was a correlation with some clinical manifestations of GD1

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsGaucher Disease
CountriesFrance
Collaborators--

Timeline

N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedJan 8, 2016
Enrollment StartJan 1, 2010
Primary CompletionDec 1, 2015
TodayJul 2, 2026
Enrollment to primary: 5.9 yearsPosted 10.5 years ago

Interventions

genetic analysesgenetic