Clinical and Genetic Testing of Patients With Usher Syndrome
NCT03319524 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 28
Last updated 2019-04-03
Summary
This study is aimed to characterize Russian population of Usher patients.
Conditions
- Usher Syndrome
- Congenital Deafness
- Retinitis Pigmentosa
Sponsors & Collaborators
-
Burnasyan Federal Medical Biophysical Center
collaborator OTHER_GOV -
Scientific and Clinical Center for Otorhinolaryngology of FMBA of Russia
collaborator UNKNOWN -
Federal State Budgetary Institution Research Center for Medical Genetics
collaborator UNKNOWN -
ANO Laboratory Sensor-Tech
collaborator UNKNOWN -
Oftalmic LLC
collaborator UNKNOWN -
Deaf-Blind Support Foundation Con-nection
collaborator UNKNOWN -
Sensor Technology for Deafblind
lead INDUSTRY
Principal Investigators
-
Vladimir N Trubilin, MD, PhD, Prof · State Research Center Burnasyan Federal Medical Biophysical Center Federal Medical-Biological Agency
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-05-17
- Primary Completion
- 2018-04-01
- Completion
- 2018-06-01
Countries
- Russia
Study Locations
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