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CLINICAL_TRIALS ClinicalTrials.gov record update

Institutional Registries of Rare Diseases at Hospital Italiano de Buenos Aires (HIBA)

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
NCT06573723
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:28:38.458541+00:00
Published At
2026-01-14T00:00:00+00:00
Record Updated At
2026-01-14
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", "Amyloidosis", "Sarcoidosis", "Phacomatosis", "Pheochromocytoma", "Paraganglioma", "Von Hippel-Lindau Disease", "Immunoglobulin G4-Related Disease", "Demyelinating Diseases", "Inborn Errors of Metabolism", "Eosinophilic Gastrointestinal Disorders", "Hypertrophic Cardiomyopathy", "Gaucher Disease", "Congenital Adrenal Hyperplasia", "Hereditary Angioedema", "Pulmonary Hypertension", "Wilson Disease", "Vascular Anomalies", "Mastocytosis", "Multiple Endocrine Neoplasia", "Inflammatory Bowel Diseases", "Prader-Willi Syndrome", "Hirschsprung Disease", "Cushing Syndrome", "HHT", "Hemorrhagic Hereditary Telangiectasia"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2026-01-14"
protocolSection.identificationModule.nctId
"NCT06573723"
protocolSection.identificationModule.officialTitle
"Institutional Registries of Rare Diseases at Hospital Italiano de Buenos Aires (HIBA)"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Rare Diseases (protocolSection.conditionsModule.conditions)
  • Amyloidosis (protocolSection.conditionsModule.conditions)
  • Sarcoidosis (protocolSection.conditionsModule.conditions)
  • Phacomatosis (protocolSection.conditionsModule.conditions)
  • Pheochromocytoma (protocolSection.conditionsModule.conditions)
  • Paraganglioma (protocolSection.conditionsModule.conditions)
  • Von Hippel-Lindau Disease (protocolSection.conditionsModule.conditions)
  • Immunoglobulin G4-Related Disease (protocolSection.conditionsModule.conditions)
  • Demyelinating Diseases (protocolSection.conditionsModule.conditions)
  • Inborn Errors of Metabolism (protocolSection.conditionsModule.conditions)
  • Eosinophilic Gastrointestinal Disorders (protocolSection.conditionsModule.conditions)
  • Hypertrophic Cardiomyopathy (protocolSection.conditionsModule.conditions)
  • Gaucher Disease (protocolSection.conditionsModule.conditions)
  • Congenital Adrenal Hyperplasia (protocolSection.conditionsModule.conditions)
  • Hereditary Angioedema (protocolSection.conditionsModule.conditions)
  • Pulmonary Hypertension (protocolSection.conditionsModule.conditions)
  • Wilson Disease (protocolSection.conditionsModule.conditions)
  • Vascular Anomalies (protocolSection.conditionsModule.conditions)
  • Mastocytosis (protocolSection.conditionsModule.conditions)
  • Multiple Endocrine Neoplasia (protocolSection.conditionsModule.conditions)
  • Inflammatory Bowel Diseases (protocolSection.conditionsModule.conditions)
  • Prader-Willi Syndrome (protocolSection.conditionsModule.conditions)
  • Hirschsprung Disease (protocolSection.conditionsModule.conditions)
  • Cushing Syndrome (protocolSection.conditionsModule.conditions)
  • HHT (protocolSection.conditionsModule.conditions)
  • Hemorrhagic Hereditary Telangiectasia (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.