Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis

Sponsor
Benjamin Terrier
Study ID
NCT04006535
Status
Recruiting
Apply to this trial

Conditions

Eligibility Criteria

Sex
ALL
Age
N/A - N/A
Healthy Volunteers
Accepted

Interventions

  • genetic analysis — GENETIC
    Saliva sample collection for genetic analysis

Study Details

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.

Key Dates

Start date
Jun 1, 2019
Status verified
Jul 2019
Primary completion
Jun 1, 2029
Completion
Jun 1, 2029

Study Design

Enrollment
100 participants (estimated)

Primary Outcome Measure

Identification of susceptibility loci and genes [ Time Frame: At the moment of enrollment ]

Central Contacts

Related Studies