data collection: Prospective data collection in a clinical data registry
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.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Diagnosis of Tuberculosis
* Age ≥ 18 years
* Capacity to provide informed consent
* Written informed consent to participate in the study
Exclusion Criteria:
* Lack of capacity to provide informed consent
* Age \< 18 years
Primary outcome measure(s)
Extrapulmonary TB: Favourable treatment outcome — December 2040 Identification of parameters that predict/are significantly associated with favorable outcome in EPTB
Drug-resistant TB: Description of treatment outcome — December 2040 Percentage of patients cured, failed, died, under/after therapy according to WHO and TBnet outcome criteria
Drug-resistant TB: Description of treatment completion — December 2040 Percentage of patients who develop serious/severe drug-related adverse events/who have to change regimen due to drug-related adverse events
Drug-susceptible TB: Mortality risk score — December 2040 Development of a TB mortality risk score, defined by a final set of predictors and a weighted scoring system based on routine clinical, radiological, microbiological, and laboratory data.
Therapeutic drug monitoring: Description of Pharmacokinetics — December 2040 Summary of pharmacokinetic parameters: Mean max/min concentrations, number of patients that are over-/under-/correctly dosed
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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