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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Register of Patients With Prader-Willi SyndromeAbnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Imprinting Disorders, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Overweight, Prader-Willi syndrome, chromosomal disorder, hereditary disease, intellectual disability, nervous system disorder, nutritional disorder, obesity disorder, overnutritionRecruitingNot stated2024-02-20NCT02829684

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OrganizationsLinked trials
University Hospital, Toulouse216

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Research sitesCityCountryLinked trials
University Hospital of ChildrenToulouseFrance1