Prospective Cohort of People Starting Treatment for Tuberculosis Disease in France (FrenchTB)

NCT06893757 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2025-03-25

No results posted yet for this study

Summary

The French Tuberculosis Cohort is a prospective, national, multicenter, low-intervention study including subjects aged 18 years and older with tuberculosis disease for which inpatient treatment is initiated. The goal of this observational study is to follow-up and anti-tuberculosis treatment will be provided according to current French recommendations. Participants will provide sociodemographic, clinical, biological, radiological and bacteriological data at various protocol visits at 2 days, 1 and 2 weeks, 2 months, at the end of treatment, 12 and 24 months. Consenting participants will have samples collected at scheduled visits for the establishment of a biobank. This will include blood, urine, breath and hair samples. The positive mycobacterial strains will constitute a specimen bank.

Conditions

Sponsors & Collaborators

  • University of Bordeaux

    collaborator OTHER
  • Amiens University Hospital

    collaborator OTHER
  • Centre National de la Recherche Scientifique, France

    collaborator OTHER
  • Saint Antoine University Hospital

    collaborator OTHER
  • University of Lyon

    collaborator OTHER
  • Claude Bernard University

    collaborator OTHER
  • University Hospital, Bordeaux

    collaborator OTHER
  • Saint-Louis Hospital, Paris, France

    collaborator OTHER
  • Centre Hospitalier Universitaire, Amiens

    collaborator OTHER
  • Hôpital Jean Verdier

    collaborator OTHER
  • Institut National de la Santé Et de la Recherche Médicale, France

    collaborator OTHER_GOV
  • ANRS, Emerging Infectious Diseases

    lead OTHER_GOV

Principal Investigators

  • Nathalie DE CASTRO, MD PHD · Hôpital Saint Louis Paris

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-30
Primary Completion
2027-06-30
Completion
2031-06-30

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06893757 on ClinicalTrials.gov