Cohort of Patients With Systemic Granulomatosis and Associated Biological Collection
NCT ID: NCT06854848
Last Updated: 2026-02-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
150 participants
OBSERVATIONAL
2025-12-04
2035-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Granulomatosis
blood sample
30 ml whole blood for Peripheral blood mononuclear cell (PBMC) and monocytes isolation
urine sample
10 ml
Interventions
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blood sample
30 ml whole blood for Peripheral blood mononuclear cell (PBMC) and monocytes isolation
urine sample
10 ml
Eligibility Criteria
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Inclusion Criteria
* Patients with systemic granulomatosis (diagnosis proven by anatomopathological sampling) at diagnosis.
* Persons affiliated to or benefiting from a social security scheme.
* Free, informed and written consent signed by the participant and the investigator (at the latest on the day of inclusion and before any examination required by the research).
Exclusion Criteria
* Pregnant or breast-feeding women
* Patients already receiving specific treatment for systemic granulomatosis
* Persons deprived of their liberty by a judicial or administrative decision, minors, persons of legal age who are the object of a legal protection measure or unable to express their consent.
18 Years
ALL
No
Sponsors
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University Hospital, Bordeaux
OTHER
Responsible Party
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Principal Investigators
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Emmanuel RIBEIRO, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Bordeaux
Locations
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CHU de Bordeaux - service de Médecine Interne et Immunologie Clinique
Bordeaux, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CHUBX 2024/73
Identifier Type: -
Identifier Source: org_study_id
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