CompletedNCT03959605
Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children
Studying Oculocutaneous albinism type 5
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Fondation Ophtalmologique Adolphe de Rothschild
- Principal Investigator
- Martine MAUGET FAYSSEFondation A. de Rothschild
- Intervention
- blood sample for genetic test(genetic)
- Enrollment
- 48 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2021
Study locations (1)
- Fondation A de Rothschild, Paris, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT03959605 on ClinicalTrials.gov