Actively Recruiting

Age: 18Years +
All Genders
NCT04413331

Prospective Longitudinal Cohort Study of Vasculitis Patients

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-09-12

670

Participants Needed

1

Research Sites

626 weeks

Total Duration

On this page

Sponsors

A

Assistance Publique - Hôpitaux de Paris

Lead Sponsor

U

URC-CIC Paris Descartes Necker Cochin

Collaborating Sponsor

AI-Summary

What this Trial Is About

VASCO is a prospective observational cohort study which aim to describe the presentation, comorbidities, management, outcomes and damage of vasculitis patients, from the analysis of the clinical, biological and immunological data.

CONDITIONS

Official Title

Prospective Longitudinal Cohort Study of Vasculitis Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged over 18 years
  • Diagnosis of vasculitis according to the Chapel Hill International Nomenclature revised in 2012
  • Inclusion at an active phase of disease, either initial flare or relapse
  • Signed informed consent
  • Pregnant and breastfeeding women allowed
  • Affiliated with a social security system (beneficiary or entitled person)
Not Eligible

You will not qualify if you...

  • Refusal or inability to give consent
  • Psychiatric or intellectual impairment preventing informed consent
  • Under guardianship or curatorship
  • Receiving state medical assistance (AME)
  • Hemoglobin less than 7 g/dl at sampling
  • Hemoglobin less than 9 g/dl at sampling if respiratory or cardiovascular disease present
  • Weighing less than 18 kg
  • Participation in an interventional protocol permitted

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Service de médecine interne, Hôpital Cochin, AP-HP

Paris, France, 75014

Actively Recruiting

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Research Team

B

Benjamin Terrier, PhD

CONTACT

M

Marie BENHAMMANI-GODARD

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

2

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