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Study identifier: NCT07531927 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Safety and Clinical Applicability of Transcorneal Electrical Stimulation (TES) in Geographic Atrophy

Condition: Geographic Atrophy Secondary to Age-related Macular Degeneration  ·  Sponsor: Okuvision GmbH

PhaseNA
Planned participants70
Who can joinAll sexes, 60 Years to no upper limit
Healthy volunteersNo

About this study

Geographic atrophy (GA) is a progressive eye disease that causes the degeneration of the retinal cells, particularly in the macula, leading to vision loss. The goal of this pilot study is to evaluate the safety and the effectiveness of transcorneal electrical stimulation (TES) therapy with the OkuStim 2 System in patients with geographic atrophy (GA). Researchers will compare the effects of two different electrical stimuli with a placebo to see if the stimuli are safe and can slow down the progression of the disease. Participants will be randomly assigned to one of these three groups: * TES-treatment with a rectangular stimulus * TES-treatment with a repetitive ramp stimulus * Placebo (sham) treatment Participants will apply the therapy at home, once a week for 30 minutes each over a duration of 1 year.

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

Talk to the study team

Ruth Schippert, PhD  ·  +49 7121 15935  ·  studies@okuvision.de

Always discuss trial participation with your own doctor first.

Locations (5)

Department of Ophthalmology, University Medical Center Hamburg-EppendorfHamburg, GermanyRecruiting
Department of Ophthalmology, Ludwig-Maximilians-University MunichMünchen, GermanyRecruiting
Department of Ophthalmology, Klinikum StuttgartStuttgart, GermanyRecruiting
Centre for Ophthalmology, University Hospital TuebingenTübingen, GermanyRecruiting
Department of Ophthalmology, University Hospital UlmUlm, GermanyNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07531927