Systemic Lupus Erythematosus Within the Framework of the Multidisciplinary Consultation

Overview

Diagnosis and follow up of a lupus cohort in a multidisciplinary consultation in Brest ( France)

Full Title of Study: “Cohort Follow-up of Systemic Lupus Erythematosus Within the Framework of the Multidisciplinary Consultation at the CHRU of Brest”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: N/A
    • Intervention Model: Single Group Assignment
    • Primary Purpose: Diagnostic
    • Masking: None (Open Label)
  • Study Primary Completion Date: May 13, 2025

Detailed Description

all patients coming to the LUPUS multidisciplinary consultation in brest ( France) will have a clinical examination, a biological and immunogical blood samples, cutaneous biopsies or renal biospies if necessary, an ultrasonographic articular and salivary glandular examination if needed. In case of articular involvement, some Xrays ( hands and feet) will be done at the inclusion and during the follow up each year during 5 years .

Interventions

  • Other: description of a lupus patient cohort
    • description of a lupus patient cohort

Arms, Groups and Cohorts

  • Other: lupus cohort follow up
    • it is a descrption lupus patients study

Clinical Trial Outcome Measures

Primary Measures

  • Cohort lupus: epidemiologic lupus study about diagnosis and follow up
    • Time Frame: five years
    • epidemiologic lupus study in collecting data ( description of the population, biologic and immunologic data collection, data of articular damges with xrays datas) about Diagnosis and follow up of a cohort lupus in a multidisciplibnary consultation in brest hospital ( France).

Participating in This Clinical Trial

Inclusion Criteria

  • women or men, more than 18 years old, coming to the multidisciplinary consultation in brest ( France). – With written consentment Exclusion Criteria:

  • patients less than 18 years old – refusing to participate – Under legal protection

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 80 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • University Hospital, Brest
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Contact(s)
    • sandrine jousse joulin, MD, +33 2 98 34 72 68, sandrine.jousse-oulin@chu-brest.fr

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