Viewing Study NCT03959605


Ignite Creation Date: 2025-12-25 @ 3:21 AM
Ignite Modification Date: 2025-12-26 @ 1:59 AM
Study NCT ID: NCT03959605
Status: COMPLETED
Last Update Posted: 2021-10-21
First Post: 2019-05-18
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children
Sponsor: Fondation Ophtalmologique Adolphe de Rothschild
Organization:

Study Overview

Official Title: Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children
Status: COMPLETED
Status Verified Date: 2021-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ALAFOR
Brief Summary: Fovea plana could be the phenoyipic translation of a genetic anomaly in one of the genes identified in albinisme
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: