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CLINICAL_TRIALS ClinicalTrials.gov record update

Deciphering MORC2 Genotype/Phenotype Correlation to Improve Patient Diagnostic

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
NCT07038239
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:27:37.444347+00:00
Published At
2025-07-04T00:00:00+00:00
Record Updated At
2025-07-04
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
["Charcot Marie Tooth Disease", "DIFGAN", "Developmental Delay (Disorder)", "Impaired Growth", "Dysmorphic Facies and Axonal Neuropathy"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-07-04"
protocolSection.identificationModule.nctId
"NCT07038239"
protocolSection.identificationModule.officialTitle
"Deciphering MORC2 Genotype/Phenotype Correlation to Improve Patient Diagnostic"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Charcot Marie Tooth Disease (protocolSection.conditionsModule.conditions)
  • DIFGAN (protocolSection.conditionsModule.conditions)
  • Developmental Delay (Disorder) (protocolSection.conditionsModule.conditions)
  • Impaired Growth (protocolSection.conditionsModule.conditions)
  • Dysmorphic Facies and Axonal Neuropathy (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.