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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Walking Program in Fatty Liver Children With PhenylketonuriaBrain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, brain disorder, central nervous system disorder, fatty liver disease, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, liver disorder, metabolic disease, metabolic dysfunction-associated steatotic liver disease, nervous system disorder, phenylketonuriaRecruitingNot applicable2024-12-05NCT06718842

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OrganizationsLinked trials
Cairo University1114

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Research sitesCityCountryLinked trials
Cairo UniversityDokkiEgypt9