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Primary ciliary dyskinesia 1
MONDO:0009484Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAI1 gene.
Also known as: CILD1, DNAI1 primary ciliary dyskinesia, ciliary dyskinesia, primary, type 1, primary ciliary dyskinesia 1, primary ciliary dyskinesia caused by mutation in DNAI1, primary ciliary dyskinesia type 1, Kartagener syndrome, PCD
6 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsBroader categories
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Scientists hunt for genes that protect the lungs
Knowledge-focused Recruiting nowThis study aims to find the genes that keep airways healthy and understand how genetic mutations cause primary ciliary dyskinesia (PCD), a rare disease that leads to serious lung problems. Researchers will study people with suspected PCD and healthy family members. The goal is to…
Sponsor: University of North Carolina, Chapel Hill • Aim: Knowledge-focused
Last updated Jul 01, 2026 00:00 UTC
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Genetic clues behind polynesian lung disease? researchers dig into patient records
Knowledge-focused Recruiting nowThis study reviews medical records of 500 Polynesian patients with bronchiectasis (widened airways) to understand why the condition is so common in French Polynesia. Researchers will look at age of onset, family history, infections, and CT scan patterns to see if a genetic cause …
Sponsor: Centre Hospitalier Intercommunal Creteil • Aim: Knowledge-focused
Last updated Jun 27, 2026 14:00 UTC
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Global study to uncover hidden ENT patterns in rare lung disease
Knowledge-focused Recruiting nowThis study follows 1000 people with Primary Ciliary Dyskinesia (PCD) across multiple countries to track ear, nose, and throat symptoms over two years. Participants continue their usual care while researchers collect data through exams and questionnaires. The goal is to better und…
Sponsor: University of Bern • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:01 UTC
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Swiss launch national database to track rare lung disease
Knowledge-focused Recruiting nowThis study is creating a national registry in Switzerland for people with primary ciliary dyskinesia (PCD), a rare lung condition. Researchers will collect information on symptoms, lung function, and treatments from up to 800 patients. The goal is to better understand the disease…
Sponsor: University of Bern • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:59 UTC