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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Exploring Lived Experiences of Families of Children With Spinal Muscular Atrophy(SMA) Type 1 Regarding Feeding and CommunicationCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Deglutition Disorders, Digestive System Diseases, Pharyngeal Diseases, Spinal Muscular Atrophies of Childhood, Spinal Muscular Atrophy Type I, central nervous system disorder, digestive system disorder, esophageal disorder, hereditary disease, inherited neurodegenerative disorder, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, otorhinolaryngologic disease, spinal cord disorder, spinal muscular atrophyNot yet recruitingNot stated2026-06-02NCT07596277