Prospective Open Clinical and Genetic Study of Patients With Retinitis Pigmentosa

Key facts

Sponsor

Sensor Technology for Deafblind

Principal Investigator

Dmitry S. Atarshchikov, MD, PhD

Central Clinical Hospital under President Affairs

Intervention

Whole Exome Sequencing(diagnostic_test)

Enrollment

130 enrolled

Eligibility

6-65 years · All sexes

Timeline

2019 – 2020

Study locations (2)

• Federal State Budgetary Institution "Moscow Helmholtz Research Institute of Eye Diseases" of the Ministry of Health, Moscow, Russia
• Central Clinical Hospital under President Affairs, Moscow, Russia

Collaborators

Central Clinical Hospital under President Affairs · Deaf-Blind Support Foundation Con-nection · Federal State Budgetary Institution Moscow Helmholtz Eye Research Institute · Federal State Budgetary Institution Research Center for Medical Genetics · Oftalmic LLC · Center for Genetics and Reproductive Medicine Genetico

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

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See all trials for OBSOLETE: Inherited retinal disorder →