Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis

Recruiting now

Conditions studied: Vasculitis

In brief

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 facts

Study ID

NCT04006535

Run by

Benjamin Terrier

People needed

100

Starts

2019-06-01

Expected to finish

2029-06-01

Last updated by the study team

2019-07-08

Who can join

Age: any. Sex: any. Healthy volunteers: accepted.

You may not qualify if…

• Refusal of consent or inability to obtain consent
• Dementia or unauthorized patient, for psychiatric or intellectual failure reasons, to receive information about the protocol and to give informed consent.
• Uncooperative patient, or any pathology that could make the patient potentially non-compliant to the study procedures, and patients interned for regulatory or legal reasons.

Where it is running

• Hôpital Cochin - Department of Internal Medicine — Paris, Île-de-France Region, France (enrolling)

Full record on ClinicalTrials.gov

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