NCT03990727View on ClinicalTrials.gov

Phenotype Correlates Genotype of Inherited Retina Dystrophies, Retinitis Pigmentosa, Con>Rod Dystrophies.

UnknownOBSERVATIONAL
Enrollment

17,000

Participants

Timeline

Start Date

August 31, 2009

Primary Completion Date

June 13, 2019

Study Completion Date

September 30, 2025

Conditions
Retinitis PigmentosaCone DystrophyUsher SyndromesRetina; Dystrophy
Interventions
DIAGNOSTIC_TEST

Retina Analysis-mosaic

Fundus retina pattern study

DIAGNOSTIC_TEST

Autofluorescence

Fundus reflectance-functionality

DIAGNOSTIC_TEST

OCT- 1 micra

Fine tomography fundus retina

PROCEDURE

Genotype analysis

Molecular target retina dystrophy analysis

Trial Locations (1)

97130

RECRUITING

Retina and Genomics Institute, Mérida

Sponsors

Lead Sponsor

MejoraVisionMD
All Listed Sponsors
collaborator

Maisonneuve-Rosemont Hospital

OTHER

collaborator

Retina and Genomics Institute

UNKNOWN

lead

MejoraVisionMD

NETWORK

NCT03990727 - Phenotype Correlates Genotype of Inherited Retina Dystrophies, Retinitis Pigmentosa, Con>Rod Dystrophies. | Biotech Hunter | Biotech Hunter