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NOT YET RECRUITING
NCT07677904

Tuberculosis Clinical Registry in Europe

Sponsor: Research Center Borstel

View on ClinicalTrials.gov

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.

Official title: Tuberculosis Clinical Registry in Europe - the TBnet Registry

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

1000

Start Date

2026-07

Completion Date

2040-12

Last Updated

2026-07-01

Healthy Volunteers

No

Conditions

Interventions

OTHER

data collection

Prospective data collection in a clinical data registry

Locations (2)

Research Center Borstel, Leibniz Lung Center

Borstel, Schleswig-Holstein, Germany

IRCCS Ospedale Sacro Cuore Don Calabria

Negrar, Verona, Italy