Menu
Recruiting NCT06522347

Mycobacteria Registry Study: Prospective Observational Study in Austria

Observational Non-Tuberculous Mycobacterial Pneumonia Tuberculosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Non-Tuberculous Mycobacterial Pneumonia, Tuberculosis. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Austria
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The goal of this non-interventional registry study is to systematically collect epidemiological and clinical data throughout the treatment course to learn about effectiveness of treatments. We will document the natural course of therapy without additional interventions. The main question to answer is: What are the risk factors for mortality due to infection with Mycobacteria tuberculosis (TB) or Nontuberculous mycobacteria (NTM) in Austria? Data from participants already receiving treatment as part of their regular medical care for TB or NTM infections will be collected.

Primary outcome measures

  • Mortality [Time frame: 30 years]
Secondary outcome measures (3)
  • Prevalence [Time frame: 30 years]
  • Patient cohort [Time frame: 30 years]
  • Risk factors [Time frame: 30 years]

Eligibility criteria

Inclusion criteria

  • patients diagnosed with Mycobacterium tuberculosis or non-tuberculous mycobacteria infection
  • individuals aged 18 years or older
  • written informed consent

Exclusion criteria

  • to not comprehend and rightfully judge participation

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Austria · 3 centers
  • Klinik Hietzing — Vienna
  • Klinik Penzing — Vienna
  • Ludwig Boltzmann Institut for Lung Health — Vienna

Identifiers

NCT: NCT06522347 · TBC-NTM

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗