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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
MRI Assessment of Lung Airways in Cystic Fibrosis: Evaluate MRI's Ability to Detect Changes in Airway Structure .Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Infant, Newborn, Diseases, cystic fibrosis, hereditary disease, lung disorder, pancreas disorder, respiratory system disorderNot yet recruitingNot stated2026-03-06NCT07454681

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OrganizationsLinked trials
The Hospital for Sick Children162

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Research sitesCityCountryLinked trials
Hospital for Sick ChildrenTorontoCanada8