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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Blood Spot and Urine Metabolomic Screening Applied to Rare DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, hereditary disease, inborn errors of metabolism, metabolic diseaseRecruitingNot applicable2024-04-12NCT06360913

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Research sitesCityCountryLinked trials
Chu LiegeLiègeBelgium2
Cliniques universitaires Saint LucBrusselsBelgium1
Hôpital Universitaire des enfants Reine Fabiola (HUDERF-ULB)BrusselsBelgium1
Institut de Pathologie et de Génétique (IPG)CharleroiBelgium2