NCT04006535

Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis

Identification of Susceptibility Loci and Genes for Systemic Vasculitis Risk, by Analyzing Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis (FAMILYVASC Study)

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 100 (estimated)
• Sponsor: Benjamin Terrier · Academic / Other
• Sex: All
• Age: —
• Healthy volunteers: Accepted

Summary

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.

Conditions

• Vasculitis

Interventions

Type	Name	Description
GENETIC	genetic analysis	Saliva sample collection for genetic analysis

Timeline

• Start date: 2019-06-01
• Primary completion: 2029-06-01
• Completion: 2029-06-01
• First posted: 2019-07-05
• Last updated: 2019-07-08

Locations

1 site across 1 country: France