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Clinical trial

Functional Study of Intronic Variants in Inherited Cone Disorders

NCT04658251 is registered in ClinicalTrials.gov with University Hospital, Lille as lead sponsor.

NCT NCT04658251
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Registry record

As filed in ClinicalTrials.gov.

Title
Functional Study of Intronic Variants in Inherited Cone Disorders
Lead sponsor
University Hospital, Lille
Phase
Observational
Overall status
Terminated
Start date
March 3, 2021
Completion date
April 14, 2024
Enrollment
7 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

cone dystrophy, cone rod dystrophy, macular degeneration, retinal dystrophy, cone-rod