Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Speech Therapy for Children With Rare Genetic Conditions and Childhood Apraxia of SpeechCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Psychomotor Disorders, Signs and Symptoms, apraxia, childhood apraxia of speech, communication disorder, hereditary disease, nervous system disorder, neurodevelopmental disorder, psychiatric disorderRecruitingNot applicable2026-09-11NCT07815249

1 results · Page 1 of 1

Swipe the table sideways for more columns.

OrganizationsLinked trials
Murdoch Childrens Research Institute56

1 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sitesCityCountryLinked trials
Murdoch Children's Research InstituteMelbourneAustralia2