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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Characterisation of a Population of Adults Suffering From Cystic Fibrosis in a Belgian Reference CenterCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Infant, Newborn, Diseases, Nutritional and Metabolic Diseases, cystic fibrosis, diabetes mellitus, endocrine system disorder, glucose metabolism disease, hereditary disease, lung disorder, metabolic disease, pancreas disorder, respiratory system disorderEnrolling by invitationNot stated2026-03-02NCT07442682