Clinical trial
Genetic Studies of Lysosomal Storage Disorders
NCT00001215 · National Human Genome Research Institute (NHGRI), NIH · Enrolling by invitation
Key facts
| NCT number | NCT00001215 |
|---|---|
| Title | Genetic Studies of Lysosomal Storage Disorders |
| Official title | Studies of Genetic Heterogeneity in Patients With Lysosomal Storage Disorders |
| Lead sponsor | National Human Genome Research Institute (NHGRI), NIH |
| Status | Enrolling by invitation |
| Study type | Observational |
| Conditions | Lysosomal Storage Disorders, Gaucher Disease, Parkinson Disease |
| Enrollment | 1,000 |
| Start date | Mar 8, 1995 |
| First posted | Nov 4, 1999 |
| Last update posted | Jan 8, 2026 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: