Transcorneal Electrical Stimulation - Multicenter Safety Study

Status Completed

Clinical Trial Summary

The purpose of this study is to expand the safety assessment of repeated applications of an electrical current from a DTL-like electrode in patients with RP.

Clinical Trial Description

This is a single-arm open label interventional safety trial with RP patients, who receive weekly TES for 6 months on 1 eye followed by observation for another 6 months without stimulation. The primary outcome measure is safety, indicated by the frequency and severity of adverse events. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01835002
Study type	Interventional
Source	Okuvision GmbH
Contact
Status	Completed
Phase	N/A
Start date	September 2012
Completion date	August 2015

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