Registry for patients with non-CF Bronchiectasis and NTM

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The Bronchiectasis Research Registry is a comprehensive database that collects information from patients diagnosed with non-cystic fibrosis (non-CF) Bronchiectasis and Nontuberculosis Mycobacteria (NTM) across various clinical institutions. Its primary aim is to facilitate collaborative research and aid in the design of multi-center clinical trials targeting these conditions. By consolidating patient data, the registry seeks to enhance understanding of the different types of Bronchiectasis and the underlying mechanisms of the disease. This initiative is a partnership with NTM Info and Research, Inc., and the COPD Foundation, focusing on improving patient outcomes through better research insights.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Over the age of 18
* non-CF Bronchiectasis
* Nontuberculosis Mycobacteria (NTM)

Exclusion Criteria:

* Under the age of 18
* CF Bronchiectasis

Where it's running

• COPD Foundation
  Washington D.C., District of Columbia, United States Recruiting

Study contacts

• Study coordinator: Delia Prieto
• Phone: 1-866-731-2673

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• A patient registry for COPD research

  This study is gathering health information from over 75,000 people with COPD to help find better treatments and a cure for the disease.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.