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Clinical trial

"Understanding Genetic Missing Variability and Pathogenetic Mechanisms of Inherited Retinal Dystrophies Using Whole Genome Sequencing and in Vitro and in Vivo Models"

NCT05793515 is registered in ClinicalTrials.gov with Istituto Superiore di Sanità as lead sponsor.

NCT NCT05793515
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Registry record

As filed in ClinicalTrials.gov.

Title
"Understanding Genetic Missing Variability and Pathogenetic Mechanisms of Inherited Retinal Dystrophies Using Whole Genome Sequencing and in Vitro and in Vivo Models"
Lead sponsor
Istituto Superiore di Sanità
Phase
Observational
Overall status
Completed
Start date
November 15, 2022
Completion date
November 2, 2024
Enrollment
120 (actual)
Sites
1

Conditions

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

inherited retinal dystrophy, macular dystrophy, retinitis pigmentosa