Catalyst Wire Dossier Catalyst Wire Dossier
CLINICAL_TRIALS ClinicalTrials.gov record update

Introduction of Tandem Mass Spectrometry (MS/MS) Technology in the Program of Selective Screening of Hereditary Metabolic Diseases in Kazakhstan

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
NCT05910151
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:39:06.728323+00:00
Published At
2023-06-18T00:00:00+00:00
Record Updated At
2023-06-18
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
["Propionic/Methylmalonic Acidemias", "Maple Syrup Urine Disease", "Citrullinemia", "Argininosuccinic Aciduria", "Ornithine Transcarbamylase Deficiency", "Carbamoyl Phosphate Synthetase I Deficiency", "N-acetylglutamate Synthase Deficiency", "Nonketotic Hyperglycinemia", "Tyrosinemia", "Homocystinuria", "Arginase Deficiency", "Isovaleric Acidemia", "Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency", "Isobutyryl-CoA Dehydrogenase Deficiency", "Glutaric Acidemia Type I", "3-methylcrotonyl-CoA Carboxylase Deficiency", "Biotinidase Deficiency", "Malonyl-CoA Decarboxylase Deficiency", "Beta-ketothiolase Deficiency", "3-hydroxy-3-methylglutaryl-CoA Lyase Deficiency", "3-methylglutaconyl-CoA Hydratase Deficiency", "Medium-chain Acyl-CoA Dehydrogenase Deficiency", "Very Long-chain Acyl-CoA Dehydrogenase Deficiency", "Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency", "Glutaric Acidemia Type II", "Primary Carnitine Deficiency", "Carnitine Palmitoyltransferase I Deficiency", "Carnitine Palmitoyltransferase II Deficiency", "Carnitine-acylcarnitine Translocase Deficiency"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2023-06-18"
protocolSection.identificationModule.nctId
"NCT05910151"
protocolSection.identificationModule.officialTitle
"Introduction of Tandem Mass Spectrometry (MS/MS) Technology in the Program of Selective Screening of Hereditary Metabolic Diseases in Kazakhstan"
protocolSection.statusModule.overallStatus
"UNKNOWN"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Propionic/Methylmalonic Acidemias (protocolSection.conditionsModule.conditions)
  • Maple Syrup Urine Disease (protocolSection.conditionsModule.conditions)
  • Citrullinemia (protocolSection.conditionsModule.conditions)
  • Argininosuccinic Aciduria (protocolSection.conditionsModule.conditions)
  • Ornithine Transcarbamylase Deficiency (protocolSection.conditionsModule.conditions)
  • Carbamoyl Phosphate Synthetase I Deficiency (protocolSection.conditionsModule.conditions)
  • N-acetylglutamate Synthase Deficiency (protocolSection.conditionsModule.conditions)
  • Nonketotic Hyperglycinemia (protocolSection.conditionsModule.conditions)
  • Tyrosinemia (protocolSection.conditionsModule.conditions)
  • Homocystinuria (protocolSection.conditionsModule.conditions)
  • Arginase Deficiency (protocolSection.conditionsModule.conditions)
  • Isovaleric Acidemia (protocolSection.conditionsModule.conditions)
  • Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency (protocolSection.conditionsModule.conditions)
  • Isobutyryl-CoA Dehydrogenase Deficiency (protocolSection.conditionsModule.conditions)
  • Glutaric Acidemia Type I (protocolSection.conditionsModule.conditions)
  • 3-methylcrotonyl-CoA Carboxylase Deficiency (protocolSection.conditionsModule.conditions)
  • Biotinidase Deficiency (protocolSection.conditionsModule.conditions)
  • Malonyl-CoA Decarboxylase Deficiency (protocolSection.conditionsModule.conditions)
  • Beta-ketothiolase Deficiency (protocolSection.conditionsModule.conditions)
  • 3-hydroxy-3-methylglutaryl-CoA Lyase Deficiency (protocolSection.conditionsModule.conditions)
  • 3-methylglutaconyl-CoA Hydratase Deficiency (protocolSection.conditionsModule.conditions)
  • Medium-chain Acyl-CoA Dehydrogenase Deficiency (protocolSection.conditionsModule.conditions)
  • Very Long-chain Acyl-CoA Dehydrogenase Deficiency (protocolSection.conditionsModule.conditions)
  • Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency (protocolSection.conditionsModule.conditions)
  • Glutaric Acidemia Type II (protocolSection.conditionsModule.conditions)
  • Primary Carnitine Deficiency (protocolSection.conditionsModule.conditions)
  • Carnitine Palmitoyltransferase I Deficiency (protocolSection.conditionsModule.conditions)
  • Carnitine Palmitoyltransferase II Deficiency (protocolSection.conditionsModule.conditions)
  • Carnitine-acylcarnitine Translocase Deficiency (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.