Tuberculosis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have a confirmed diagnosis of cystic fibrosis (CF)
- People of any age, including children (with consent provided by a parent or legal guardian)
- People for whom written consent to take part in the study has been given (either by the person themselves, or by a parent or legal guardian for children)
- People who have a certain type of lung infection called NTM (non-tuberculous mycobacteria) — if this applies, the infection must have been diagnosed using recognised medical guidelines, and a sample of the bacteria must be available for testing (confirm with trial site)
Who may not be able to join:
- People who are unable to give informed consent, who do not wish to take part, or who have chosen to withdraw their consent to participate
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Alexander Mischnik, Prof. Dr. med., National and WHO-Supranational Reference Center for Mycobacteria, Research Center Borstel, Leibniz Lung Center
Phone: +49 4537 / 188-7540
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Prevalence of NTM in environmental samples; Difference in NTM prevalence between case and control groups; Genetic concordance between environmental and patient isolates
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.