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Starting soon Observational

Tuberculosis Clinical Registry in Europe

NCT07677904 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2026-07
Last updated
2026-07-01

Condition(s) studied

Tuberculosis

Investigational drug(s) / intervention(s)

data collection

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

Trial sites (2)

FacilityCityRegionStatus
Research Center Borstel, Leibniz Lung Center Borstel Schleswig-Holstein
IRCCS Ospedale Sacro Cuore Don Calabria Negrar Verona
Official registry record

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.

View NCT07677904 on ClinicalTrials.gov ↗ ← All trials in Italy