Swiss launch national database to track rare lung disease
NCT ID NCT03606200
First seen Dec 11, 2025 · Last updated May 24, 2026 · Updated 24 times
Summary
This study is a national registry that collects health information from people in Switzerland who have Primary Ciliary Dyskinesia (PCD), a rare lung condition. Researchers will track symptoms, lung function, treatments, and test results over time. The goal is to better understand the disease and support future research. No new treatments are being tested.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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University of Bern
RECRUITINGBern, 3012, Switzerland
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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