Trials / NCT03990727
Phenotype Correlates Genotype of Inherited Retina Dystrophies, Retinitis Pigmentosa, Con>Rod Dystrophies.
Status unknown Observational Natural history / observational
- Sponsor
- MejoraVisionMD
- Treatment
- Retina Analysis-mosaic; Autofluorescence; OCT- 1 micra; Genotype analysis
- Gene
- Not stated
- Conditions
- Retinitis Pigmentosa, Cone Dystrophy, Usher Syndromes, Retina; Dystrophy
- Ages
- 2 Weeks to 90 Years
- Enrollment
- 17000 participants
- Started
- 2009-08
- Main results expected
- 2019-06-13
- Results posted
- Not yet
- Record last updated
- 2019-06-19
What the study is testing
Patients with retina dystrophies (retinitis pigmentosa, cone>rods dystrophies, Usher and syndromic) will be correlated with genotype and validate inheritance mode by segregation analysis.
Where it runs
Mexico (1)
- Retina and Genomics Institute, Mérida, Yucatán (recruiting now)