Clinical trial
Genetic Analysis of Oculocerebrorenal Syndrome of Lowe
NCT00359515 · National Human Genome Research Institute (NHGRI), NIH · Completed
Key facts
| NCT number | NCT00359515 |
|---|---|
| Title | Genetic Analysis of Oculocerebrorenal Syndrome of Lowe |
| Official title | Mutation Detection for Lowe Syndrome |
| Lead sponsor | National Human Genome Research Institute (NHGRI), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Lowe Syndrome |
| Enrollment | 120 |
| Start date | Feb 17, 2001 |
| Completion | Feb 3, 2009 |
| First posted | Aug 2, 2006 |
| Last update posted | Jul 2, 2017 |
| 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: