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CLINICAL_TRIALS ClinicalTrials.gov record update

Identification of the Molecular and/or Pathophysiological Bases of Rare Diseases of Genetic Origin (or Rare Forms of Frequent Diseases Suspected of Being of Genetic Origin).

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT03287193
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:28:52.383468+00:00
Published At
2025-12-08T00:00:00+00:00
Record Updated At
2025-12-08
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
["Rare Diseases of Genetic Origin", "Rare Forms of Common Diseases Suspected of Being Genetic in Origin"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-12-08"
protocolSection.identificationModule.nctId
"NCT03287193"
protocolSection.identificationModule.officialTitle
"Identification of the Molecular and/or Pathophysiological Bases of Rare Diseases of Genetic Origin (or Rare Forms of Frequent Diseases Suspected of Being of Genetic Origin)."
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Rare Diseases of Genetic Origin (protocolSection.conditionsModule.conditions)
  • Rare Forms of Common Diseases Suspected of Being Genetic in Origin (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.