Swiss database tracks rare lung disease to unlock future treatments
NCT ID NCT03606200
Summary
This study is a national patient registry, not a treatment trial. It aims to collect long-term health information from up to 800 people in Switzerland who have Primary Ciliary Dyskinesia (PCD), a rare genetic condition affecting the lungs and sinuses. By tracking symptoms, treatments, and health outcomes over time, researchers hope to better understand the disease and create a platform to support future research and clinical trials.
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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
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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