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NCT03959605: ALAFOR

Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children

Completed Last updated 21 October 2021
What this trial tests

trial testing blood sample for genetic test in Albinism, Ocular in 48 participants. Completed in 1 October 2021.

Timeline
6 January 2019
Primary endpoint
2 February 2021
1 October 2021

Quick facts

Lead sponsorFondation Ophtalmologique Adolphe de Rothschild
StatusCompleted
Study typeOBSERVATIONAL
Enrollment48
Start date6 January 2019
Primary completion2 February 2021
Estimated completion1 October 2021
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Fondation Ophtalmologique Adolphe de Rothschild — full company profile →

Who can join

18 and older, any sex, with Albinism, Ocular. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Fovea plana could be the phenoyipic translation of a genetic anomaly in one of the genes identified in albinisme

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Albinism, Ocular

Currently open trials in the same condition.

Other Fondation Ophtalmologique Adolphe de Rothschild trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03959605.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing