Hôpital Cochin - Department of Internal Medicine
Paris, Île-de-France Region, 75014, France
Location status: Recruiting
NCT Number: NCT04006535
The FAMILYVASC study is a prospective observational study which will aim to identify susceptibility loci and genes for systemic vasculitis risk in patients with familial or pediatric forms of vasculitis. Genetic analysis based on whole exome sequencing will be carried out through salivary DNA.
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Observational
Paris, Île-de-France Region, 75014, France
Location status: Recruiting
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
for subjects with vasculitis
Inclusion criteria
for healthy subjects
Exclusion criteria
Saliva sample collection for genetic analysis
Time frame: At the moment of enrollment
Contact information is provided by the study sponsor or research team.
Benjamin Terrier, MD, PhD
CONTACT
Hicham Kardaoui, MSc
CONTACT
Benjamin Terrier
Other
Identification of Susceptibility Loci and Genes for Systemic Vasculitis Risk, by Analyzing Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis (FAMILYVASC Study)
Acronym: FAMILYVASC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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