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Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis

NCT04006535 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2019-07-08

No results posted yet for this 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.

Conditions

  • Vasculitis

Interventions

GENETIC

genetic analysis

Saliva sample collection for genetic analysis

Sponsors & Collaborators

  • Benjamin Terrier

    lead OTHER

Principal Investigators

  • Benjamin Terrier, MD, PhD · French Vasculitis Study Group

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-06-01
Primary Completion
2029-06-01
Completion
2029-06-01

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04006535 on ClinicalTrials.gov