# Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children

> **NCT03959605** · — · COMPLETED · sponsor: **Fondation Ophtalmologique Adolphe de Rothschild** · enrollment: 48 (actual)

## Conditions studied

- Albinism, Ocular

## Interventions

- **GENETIC:** blood sample for genetic test
- **DIAGNOSTIC_TEST:** Ophtalmological examination

## Key facts

- **NCT ID:** NCT03959605
- **Lead sponsor:** Fondation Ophtalmologique Adolphe de Rothschild
- **Sponsor class:** NETWORK
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2019-01-06
- **Primary completion:** 2021-02-02
- **Final completion:** 2021-10-01
- **Target enrollment:** 48 (ACTUAL)
- **Last updated:** 2021-10-21


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03959605

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03959605, "Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children". Retrieved via AI Analytics 2026-07-26 from https://api.ai-analytics.org/clinical/NCT03959605. Licensed CC0.

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