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CLINICAL_TRIALS ClinicalTrials.gov record update

Investigation Into the Natural History and Metabolic and Molecular Basis of RASopathies.

This page presents selected fields from the linked source record. It does not add a medical interpretation.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT04395495
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:28:47.286633+00:00
Published At
2025-12-18T00:00:00+00:00
Record Updated At
2025-12-18
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
["RAS Mutation", "Neurofibromatosis 1", "Noonan Syndrome", "Noonan Syndrome With Multiple Lentigines", "Noonan Neurofibromatosis Syndrome", "Cardiofaciocutaneous Syndrome", "Costello Syndrome", "Legius Syndrome", "Smith-Kingsmore Syndrome", "MTOR Gene Mutation", "GATOR-1 Gene Mutation", "SYNGAP1-Related Intellectual Disability", "DLG4", "MAPK1 Gene Mutation"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-12-18"
protocolSection.identificationModule.nctId
"NCT04395495"
protocolSection.identificationModule.officialTitle
"Investigation Into the Natural History and Metabolic and Molecular Basis of RASopathies."
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • RAS Mutation (protocolSection.conditionsModule.conditions)
  • Neurofibromatosis 1 (protocolSection.conditionsModule.conditions)
  • Noonan Syndrome (protocolSection.conditionsModule.conditions)
  • Noonan Syndrome With Multiple Lentigines (protocolSection.conditionsModule.conditions)
  • Noonan Neurofibromatosis Syndrome (protocolSection.conditionsModule.conditions)
  • Cardiofaciocutaneous Syndrome (protocolSection.conditionsModule.conditions)
  • Costello Syndrome (protocolSection.conditionsModule.conditions)
  • Legius Syndrome (protocolSection.conditionsModule.conditions)
  • Smith-Kingsmore Syndrome (protocolSection.conditionsModule.conditions)
  • MTOR Gene Mutation (protocolSection.conditionsModule.conditions)
  • GATOR-1 Gene Mutation (protocolSection.conditionsModule.conditions)
  • SYNGAP1-Related Intellectual Disability (protocolSection.conditionsModule.conditions)
  • DLG4 (protocolSection.conditionsModule.conditions)
  • MAPK1 Gene Mutation (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.