Trials / Completed
CompletedNCT03959605
Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 48 (actual)
- Sponsor
- Fondation Ophtalmologique Adolphe de Rothschild · Network
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Fovea plana could be the phenoyipic translation of a genetic anomaly in one of the genes identified in albinisme
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| GENETIC | blood sample for genetic test | detection of pathogenic variants among the 19 genes known to be involved in albinism |
| DIAGNOSTIC_TEST | Ophtalmological examination | measurement of visual acuity, OCT and OCTA |
Timeline
- Start date
- 2019-01-06
- Primary completion
- 2021-02-02
- Completion
- 2021-10-01
- First posted
- 2019-05-22
- Last updated
- 2021-10-21
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT03959605. Inclusion in this directory is not an endorsement.