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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Pilot Study for Systematic Neonatal Screening for Lysosomal Storage Diseases Using Tandem Mass SpectrometryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, lysosomal storage disease, metabolic diseaseRecruitingNot stated2026-05-27NCT04393701

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2 results · Page 1 of 1

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Research sitesCityCountryLinked trials
Caen University hospitalCaenFrance17
Rouen University HospitalRouenFrance14