Trials / NCT03901391
Prospective Open Clinical and Genetic Study of Patients With Retinitis Pigmentosa
Completed Observational Natural history / observational
- Sponsor
- Sensor Technology for Deafblind
- Treatment
- Whole Exome Sequencing
- Gene
- Not stated
- Conditions
- Retinitis Pigmentosa, Usher Syndromes
- Ages
- 6 Years to 65 Years
- Enrollment
- 130 participants
- Started
- 2019-03-26
- Main results expected
- 2020-10-19
- Results posted
- Not yet
- Record last updated
- 2022-05-20
What the study is testing
This study is aimed to characterize Russian population of Retinitis Pigmentosa
Where it runs
Russia (2)
- Federal State Budgetary Institution "Moscow Helmholtz Research Institute of Eye Diseases" of the Ministry of Health, Moscow
- Central Clinical Hospital under President Affairs, Moscow