CLINICAL_TRIALS
ClinicalTrials.gov record update
ScreenPlus: A Comprehensive, Flexible, Multi-disorder Newborn Screening Program
This page presents selected fields from the linked source record. It does not add a medical interpretation.
Record identity and dates
- Source
- ClinicalTrials.gov
- Source record ID
- NCT05368038
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-25T22:27:19.120812+00:00
- Published At
- 2025-09-12T00:00:00+00:00
- Record Updated At
- 2025-09-12
- Timestamp Basis
- source retrieval time was not retained by the feed adapter
- Date limitation
- source retrieval time was not retained by the feed adapter
Fields recorded by this source
- protocolSection.conditionsModule.conditions
["Acid Sphingomyelinase Deficiency", "Ceroid Lipofuscinosis, Neuronal, 2", "Cerebrotendinous Xanthomatosis", "Fabry Disease", "GM1 Gangliosidosis", "Gaucher Disease", "Lysosomal Acid Lipase Deficiency", "Metachromatic Leukodystrophy", "Mucopolysaccharidosis II", "Mucopolysaccharidosis III-B", "Mucopolysaccharidosis IV A", "Mucopolysaccharidosis VI", "Mucopolysaccharidosis VII", "Niemann-Pick Disease, Type C"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-09-12"- protocolSection.identificationModule.nctId
"NCT05368038"- protocolSection.identificationModule.officialTitle
"ScreenPlus: A Comprehensive, Flexible, Multi-disorder Newborn Screening Program"- protocolSection.statusModule.overallStatus
"ENROLLING_BY_INVITATION"- protocolSection.designModule.phases
[]- protocolSection.statusModule.resultsFirstPostDateStruct.date
""
Study condition terms
Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.
This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.