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Search / Trial NCT06893757

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

Launched by ANRS, EMERGING INFECTIOUS DISEASES · Mar 18, 2025

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Infectious Diseases Tuberculosis Clinical Social Sciences Public Health Comorbidities Epidemiology Treatment And Care Transmission France Biobank Mycobacterial Collection Cohort Prospective

ClinConnect Summary

The French Tuberculosis Cohort study, also known as FrenchTB, is designed to follow people who have recently been diagnosed with tuberculosis (TB) and are starting treatment. This study aims to collect various health information over time to better understand how TB treatments work. Participants will be adults aged 18 and older who have been diagnosed with TB and are beginning their treatment. They will need to provide consent to join the study, and if they are unable to do so, a family member may give consent for them in certain serious cases.

If you join the study, you will attend several scheduled visits over the course of your treatment, where healthcare professionals will collect information about your health and may take samples like blood, urine, and even hair. This study is not yet recruiting participants, so it’s important to check back for updates if you or a loved one are interested. Your involvement will help researchers learn more about TB and improve treatment for future patients.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Aged ≥18 years.
  • Diagnosis of tuberculosis by microbiological or clinical means, including on the basis of a pathological examination for extrapulmonary tuberculosis leading to a Compulsory Declaration (CD) and treated for less than 8 days.
  • Have signed a voluntary, informed and written consent (at the latest on the day of inclusion and before any examination carried out as part of the research), or alternatively, consent from relatives in cases of tuberculous meningitis or other serious forms of tuberculosis with impaired consciousness or confusion, until the person is able to give their consent.
  • Exclusion Criteria:
  • Presence of significant cognitive impairment that, in the opinion of the site investigator or designated person, may affect the ability to give reliable informed consent (except in the specific case of meningeal tuberculosis).

About Anrs, Emerging Infectious Diseases

ANRS, the French National Agency for Research on AIDS and Viral Hepatitis, is a prominent research organization dedicated to advancing scientific knowledge and public health responses to emerging infectious diseases. With a focus on enhancing understanding, prevention, and treatment of viral infections, ANRS conducts and supports innovative clinical trials that address urgent health challenges. By fostering collaboration among researchers, healthcare professionals, and institutions, ANRS aims to translate research findings into effective strategies that improve patient outcomes and inform public health policies. Their commitment to addressing the dynamic landscape of infectious diseases positions them as a leader in global health research.

Locations

Patients applied

0 patients applied

Trial Officials

Nathalie DE CASTRO, MD PHD

Principal Investigator

Hôpital Saint Louis Paris

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported