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Recruiting Observational

Cohort of Patients With Systemic Granulomatosis and Associated Biological Collection

NCT06854848 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-12-04
Last updated
2026-02-03

Condition(s) studied

Granulomatosis

Investigational drug(s) / intervention(s)

blood sample →urine sample →

blood sample: 30 ml whole blood for Peripheral blood mononuclear cell (PBMC) and monocytes isolation

urine sample: 10 ml

Study summary

The GRAMI-BIO study is a prospective single-centre cohort study to recruit 150 patients followed up in the the Bordeaux University Hospital. The total duration of the GRAMI-BIO study is ten years (five years of inclusion with five years of follow-up): Consecutive inclusion of patients meeting the definition of systemic granulomatosis. The main objective of this cohort is to describe to clinical progression of systemic granulomatosis and to collect blood fraction samples (serum bank, plasma bank, urine bank, DNA bank) from subjects participating in the cohort.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients aged 18 or over * 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: * Patients infected with human immunodeficiency virus (HIV), Hepatitis B virus (HBV) and/or Hepatitis C virus (HCV) * 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.

Primary outcome measure(s)

  • Describe the clinical progression of systemic granulomatosis — At baseline (Day 0) and 60 months after baseline

Trial sites (1)

FacilityCityRegionStatus
CHU de Bordeaux - service de Médecine Interne et Immunologie Clinique Bordeaux France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06854848 on ClinicalTrials.gov ↗ ← All trials in France