RP Cure Tracker

Trials / NCT07548944

Observational Study to Investigate the Short-term Effects of Transcorneal Electrical Stimulation on Visual Performance

Recruiting now Observational Natural history / observational

Sponsor
Okuvision GmbH
Treatment
Transcorneal Electrical Stimulation using the OkuStim System
Gene
Not stated
Conditions
Retinitis Pigmentosa (RP), Usher Syndrome, Cone Rod Dystrophy
Ages
18 Years to no upper limit
Enrollment
30 participants
Started
2026-04-20
Main results expected
2027-03
Results posted
Not yet
Record last updated
2026-05-01

What the study is testing

Retinitis pigmentosa and similar degenerative diseases of the retina lead to progressive loss of vision. TES therapy with the CE-marked OkuStim® System is a treatment approved in the EU for slowing the progression of the disease. Patients increasingly report short-term subjective improvements in vision, which have not yet been systematically investigated. This exploratory study is conducted to determine whether these subjective short-term effects can be measured, and therefore also be quantified, by objective tests.

Where it runs

Germany (1)

Open on ClinicalTrials.gov for contacts and eligibility