Plain-English translation of NCT06522347 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a registry study — a way of collecting real-world medical information from people already receiving treatment for tuberculosis or non-tuberculous mycobacterial infections. Researchers will gather data about your treatment and health outcomes over time to understand what factors help predict how well people do with these infections.
Doctors want to better understand which patients are at higher risk of serious complications from these infections, and what factors influence treatment success. By studying many patients' experiences, researchers can identify patterns that help predict outcomes and improve care.
You likely qualify if…
You likely don't qualify if…
You would allow researchers to collect information from your medical records as you continue your regular treatment with your doctor — no extra visits or special procedures are needed. Your health information will be documented throughout your treatment course to track how your infection progresses and how you respond to the medicines you're already taking.
AI-generated summary from trial data · Jun 3, 2026 · Not medical advice
Austria
Collaborators
Sigmund Freud PrivatUniversitat
Enrollment target
~1,000 participants
Started
January 2023
Primary completion
December 2053
Age range
18 Years and older
Last updated on clinicaltrials.gov in July 2024.
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.