Clinical trial
Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From…
NCT00422721 · Nantes University Hospital, Other · Completed
Key facts
| NCT number | NCT00422721 |
|---|---|
| Title | Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy |
| Official title | Genetical, Multi-center, Prospective Study of Phenotyping and Genotyping of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy in the Aim of the Realisation of a Clinical Trial of Gene Therapy |
| Lead sponsor | Nantes University Hospital, Other |
| Status | Completed |
| Study type | Interventional |
| Conditions | Amaurosis, Retinal Diseases |
| Intervention type | Procedure |
| Interventions | realization of a family tree, refractometry, evaluation of the presence of a nystagmus, ocular behavior, test of baby vision, test of keenness, reading test, visual field, color vision, electroretinographical activity and 4 more |
| Enrollment | 360 |
| Start date | Apr 1, 2007 |
| First posted | Jan 17, 2007 |
| Last update posted | Nov 24, 2011 |
| Countries | France |
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: