# Registry of Patients Diagnosed With Lysosomal Storage Diseases

> **NCT05619900** · — · RECRUITING · sponsor: **University of California, San Francisco** · enrollment: 250 (estimated)

## Conditions studied

- Mucopolysaccharidosis I
- Mucopolysaccharidosis II
- Mucopolysaccharidosis IV A
- Mucopolysaccharidosis VI
- Mucopolysaccharidosis VII
- Pompe Disease Infantile-Onset
- Neuronopathic Gaucher Disease
- Wolman Disease

## Interventions

- **OTHER:** There is no intervention

## Key facts

- **NCT ID:** NCT05619900
- **Lead sponsor:** University of California, San Francisco
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2022-05-31
- **Primary completion:** 2050-05-31
- **Final completion:** 2050-05-31
- **Target enrollment:** 250 (ESTIMATED)
- **Last updated:** 2026-04-08


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05619900

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05619900, "Registry of Patients Diagnosed With Lysosomal Storage Diseases". Retrieved via AI Analytics 2026-07-03 from https://api.ai-analytics.org/clinical/NCT05619900. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
