Prospective Open Clinical and Genetic Study of Patients With Retinitis Pigmentosa

CompletedOBSERVATIONAL
Enrollment

130

Participants

Timeline

Start Date

March 26, 2019

Primary Completion Date

October 19, 2020

Study Completion Date

October 20, 2020

Conditions
Retinitis PigmentosaUsher Syndromes
Interventions
DIAGNOSTIC_TEST

Whole Exome Sequencing

Whole Exome Sequencing

Trial Locations (2)

105062

"Federal State Budgetary Institution Moscow Helmholtz Research Institute of Eye Diseases of the Ministry of Health", Moscow

121359

Central Clinical Hospital under President Affairs, Moscow

All Listed Sponsors
collaborator

Central Clinical Hospital under President Affairs

UNKNOWN

collaborator

Deaf-Blind Support Foundation Con-nection

UNKNOWN

collaborator

Federal State Budgetary Institution Moscow Helmholtz Eye Research Institute

UNKNOWN

collaborator

Federal State Budgetary Institution Research Center for Medical Genetics

UNKNOWN

collaborator

Oftalmic LLC

UNKNOWN

collaborator

Center for Genetics and Reproductive Medicine Genetico

UNKNOWN

lead

Sensor Technology for Deafblind

INDUSTRY

NCT03901391 - Prospective Open Clinical and Genetic Study of Patients With Retinitis Pigmentosa | Biotech Hunter | Biotech Hunter