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Tuberculosis Clinical Registry in Europe

NCT07677904 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2026-07-01

No results posted yet for this study

Summary

The TBnet registry is a multinational, prospective tuberculosis registry established by the Tuberculosis Network European Trialsgroup (TBnet e.V.) to collect and analyze long-term data from TB patients across Europe. Its purpose is to centralize data on TB epidemiology, prevention, diagnosis, and treatment to improve care, support research, and ultimately help eliminate TB. The registry captures risk factors, diagnostic details (e.g., microbiology, imaging, drug resistance), treatment data, side effects, outcomes, and late complications.

Conditions

Interventions

OTHER

data collection

Prospective data collection in a clinical data registry

Sponsors & Collaborators

  • European Society of Clinical Microbiology and Infectious Diseases

    collaborator OTHER

  • Tuberculosis Network European Trialsgroup (TBnet e.V.)

    collaborator UNKNOWN

  • Research Center Borstel

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-31
Primary Completion
2040-12-31
Completion
2040-12-31

Countries

  • Germany
  • Italy

Study Locations

More Related Trials

Entities

Diseases

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 NCT07677904 on ClinicalTrials.gov