Actively Recruiting
Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis
Led by Benjamin Terrier · Updated on 2019-07-08
100
Participants Needed
1
Research Sites
521 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
Official Title
Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children and adults
- Patients with vasculitis as defined by the 2012 revised Chapel Hill International Classification
- Patient information and signed informed consent
- Pregnant and breastfeeding women can be included
- Children and adults without vasculitis
- Relatives up to 4th degree of a patient with vasculitis
- Patient information and signed informed consent
- Pregnant and breastfeeding women can be included
You will not qualify if you...
- Refusal or inability to provide consent
- Dementia or inability to understand the protocol due to psychiatric or intellectual reasons
- Uncooperative patients or those with conditions that may cause non-compliance
- Patients detained for legal or regulatory reasons
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hôpital Cochin - Department of Internal Medicine
Paris, Île-de-France Region, France, 75014
Actively Recruiting
Research Team
B
Benjamin Terrier, MD, PhD
CONTACT
H
Hicham Kardaoui, MSc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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