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Ciliary Motility Disorders clinical trials

View clinical trials related to Ciliary Motility Disorders.

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NCT ID: NCT03801395 Active, not recruiting - Clinical trials for Primary Ciliary Dyskinesia

PCD New Gene Discovery

Start date: January 7, 2019
Phase:
Study type: Observational

This is a new gene discovery program for individuals with PCD who do not have a specific genetic etiology identified. Research procedures involve a single blood draw from the affected individual and from unaffected family members in an effort to identify new genetic targets.

NCT ID: NCT03704896 Active, not recruiting - Clinical trials for Primary Ciliary Dyskinesia

PRospective Observational Multicentre Study on VAriability of Lung Function in Stable PCD Patients

PROVALF-PCD
Start date: August 23, 2017
Phase:
Study type: Observational

Using routinely collected clinical data, this study aims to quantify intra-individual (i.e. in the same individual) variations between measurements of lung function in stable patients with primary ciliary dyskinesia (PCD), a rare genetic disease that causes lung damage.