European Registry Collects Long-Term Data From People With Tuberculosis
Collects information on tuberculosis patients across Europe, including treatment, side effects and outcomes.
Plain-language title generated from the registry record
Registry title: Tuberculosis Clinical Registry in Europe
Key facts
- Where
- Borstel, GermanySee the site
Where in Germany
- Research Center Borstel, Leibniz Lung CenterBorstel, GermanyNo longer taking part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Research Center Borstel
- Trial code
- NCT07677904
- Record updated
- 1 July 2026
- Original description
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.Read full original descriptionShow less
Tuberculosis Clinical Registry in Europe - the TBnet Registry
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.
Inclusion: Diagnosis of Tuberculosis; Age ≥ 18 years; Capacity to provide informed consent; Written informed consent to participate in the study.
Exclusion: Age < 18 years; Lack of capacity to provide informed consent.