Catalyst Wire Dossier Catalyst Wire Dossier
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.

Open original source record ↗

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

  • Acid Sphingomyelinase Deficiency (protocolSection.conditionsModule.conditions)
  • Ceroid Lipofuscinosis, Neuronal, 2 (protocolSection.conditionsModule.conditions)
  • Cerebrotendinous Xanthomatosis (protocolSection.conditionsModule.conditions)
  • Fabry Disease (protocolSection.conditionsModule.conditions)
  • GM1 Gangliosidosis (protocolSection.conditionsModule.conditions)
  • Gaucher Disease (protocolSection.conditionsModule.conditions)
  • Lysosomal Acid Lipase Deficiency (protocolSection.conditionsModule.conditions)
  • Metachromatic Leukodystrophy (protocolSection.conditionsModule.conditions)
  • Mucopolysaccharidosis II (protocolSection.conditionsModule.conditions)
  • Mucopolysaccharidosis III-B (protocolSection.conditionsModule.conditions)
  • Mucopolysaccharidosis IV A (protocolSection.conditionsModule.conditions)
  • Mucopolysaccharidosis VI (protocolSection.conditionsModule.conditions)
  • Mucopolysaccharidosis VII (protocolSection.conditionsModule.conditions)
  • Niemann-Pick Disease, Type C (protocolSection.conditionsModule.conditions)

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.