Trial Details
RECRUITINGBasic Information
| Clinical ID | c472 |
|---|---|
| Identifier | NCT06573723 |
| Trial Title | Institutional Registry of Rare Diseases |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NO |
|---|---|
| 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 |
| Interventions | - |
Participant Information
| Sponsor | Hospital Italiano de Buenos Aires |
|---|---|
| City | Buenos Aires |
| Country/Region | Argentina |
Enrollment Criteria
| Sex Requirement | ALL |
|---|---|
| Age Requirement | CHILD, ADULT, OLDER_ADULT |
Study Design
| Study Type | OBSERVATIONAL |
|---|---|
| Phase | NULL |
Time Information
| Start Date | 2024-07-01 |
|---|---|
| Primary Completion Date | 2034-12-31 |
| Completion Date | 2034-12-31 |