Clinical trial
Institutional Registry of Rare Diseases
NCT06573723
Study timeline
Study start (actual)2024-07-01Date precision: day
Registry last updated2026-01-14
Observed by CureCurrent2026-10-07
Recorded dates are source observations, not predictions. Missing milestones are not estimated.
Conditions
Rare Diseasesunresolved
Amyloidosisunresolved
Sarcoidosisunresolved
Phacomatosisunresolved
Pheochromocytomaunresolved
Paragangliomaunresolved
Von Hippel-Lindau Diseaseunresolved
Immunoglobulin G4-Related Diseaseunresolved
Demyelinating Diseasesunresolved
Inborn Errors of Metabolismunresolved
Eosinophilic Gastrointestinal Disordersunresolved
Hypertrophic Cardiomyopathyunresolved
Gaucher Diseaseunresolved
Congenital Adrenal Hyperplasiaunresolved
Hereditary Angioedemaunresolved
Pulmonary Hypertensionunresolved
Wilson Diseaseunresolved
Vascular Anomaliesunresolved
Mastocytosisunresolved
Multiple Endocrine Neoplasiaunresolved
Inflammatory Bowel Diseasesunresolved
Prader-Willi Syndromeunresolved
Hirschsprung Diseaseunresolved
Cushing Syndromeunresolved
HHTunresolved
Hemorrhagic Hereditary Telangiectasiaunresolved
Interventions
Sponsors & collaborators
Hospital Italiano de Buenos Aireslead sponsor
Registry source
Open the source record to verify current eligibility, contacts, locations and registry updates.
Open NCT06573723 on ClinicalTrials.gov ↗Registry-derived research relationships: ClinicalTrials.gov. Raw condition and intervention labels remain distinct from canonical MONDO/RxNorm entities unless separately normalized.