Transcorneal Electrical Stimulation - Multicenter Safety Study

NACompletedINTERVENTIONAL

Enrollment

105

Participants

Timeline

Start Date

September 30, 2012

Primary Completion Date

July 31, 2014

Study Completion Date

August 31, 2015

Conditions

Retinitis Pigmentosa

Interventions

DEVICE

Transcorneal electrostimulation

Weekly stimulation for 30 minutes with current of TES delivered of 150% of the individual phosphene threshold.

Trial Locations (7)

University Eye Clinic Bonn, Bonn

Zentrum für seltene Netzhauterkrankungen, AugenZentrum Siegburg, Siegburg

Centre for Ophthalmology at the eye clinic Tübingen, Tübingen

University Eye Clinic Regensburg, Regensburg

Glostrup Hospital and Kennedy Center, Glostrup Municipality

Augenzentrum München, Munich

Oslo University Hospital, Oslo

All Listed Sponsors

lead

Okuvision GmbH

INDUSTRY

NCT01835002 - Transcorneal Electrical Stimulation - Multicenter Safety Study | Biotech Hunter | Biotech Hunter