# Institutional Registry of Rare Diseases

> **NCT06573723** · — · RECRUITING · sponsor: **Hospital Italiano de Buenos Aires** · enrollment: 380 (estimated)

## Conditions studied

- 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

_None listed._

## Key facts

- **NCT ID:** NCT06573723
- **Lead sponsor:** Hospital Italiano de Buenos Aires
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2024-07-01
- **Primary completion:** 2034-12-31
- **Final completion:** 2034-12-31
- **Target enrollment:** 380 (ESTIMATED)
- **Last updated:** 2026-01-14


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06573723

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06573723, "Institutional Registry of Rare Diseases". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT06573723. Licensed CC0.

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