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Study identifier: NCT07228793 Synced from ClinicalTrials.gov · July 28, 2026
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Natural History Study of Patients With EYS-Associated RP

Condition: Retinitis Pigmentosa · Eye Diseases  ·  Sponsor: Sensor Technology for Deafblind

PhaseN/A
Planned participants45
Who can joinAll sexes, 14 Years to 100 Years
Healthy volunteersNo

About this study

This natural history study of patients with EYS mutations from Russia and former CIS (Commonwealth of Independent States) territories will accelerate the development of outcome measures for clinical trials. Sensitive, reliable outcome measures of retinal degeneration will greatly facilitate development of treatments for retinitis pigmentosa due to EYS mutations. This approach helps to develop experimental treatment protocol, and assessing its effectiveness. The goals and expected impact of this natural history study are to: 1. Describe the natural history of retinal degeneration in patients with biallelic mutations in EYS gene in Russia and former CIS territories. 2. Identify sensitive structural and functional outcome measures to use for future multicenter clinical trials in EYS-related retinal degeneration in Russia and former CIS territories. 3. Identify well-defined subpopulations for future clinical trials of investigative treatments for EYS-related retinal degeneration in Russia and former CIS territories.

This description comes directly from the study's public registry record.

Talk to the study team

Olga Luneva  ·  +7 9629412912  ·  info@oftalmic.com

Always discuss trial participation with your own doctor first.

Locations (1)

Oftalmic Clinical Research CenterMoscow, RussiaRecruiting

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Source record: clinicaltrials.gov/study/NCT07228793