Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis
Condition(s) studied
Investigational drug(s) / intervention(s)
genetic analysis: Saliva sample collection for genetic analysis
Study 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.
Eligibility
Primary outcome measure(s)
- Identification of susceptibility loci and genes — At the moment of enrollment
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Hôpital Cochin - Department of Internal Medicine | Paris | Île-de-France Region | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04006535 on ClinicalTrials.gov ↗ ← All trials in France