Ignite Creation Date:
2024-05-06 @ 1:33 AM
Last Modification Date:
2024-10-26 @ 11:05 AM
Study NCT ID:
NCT01835002
Status:
COMPLETED
Last Update Posted:
2021-03-04
First Post:
2013-04-15
Brief Title:
Transcorneal Electrical Stimulation - Multicenter Safety Study
Sponsor:
Okuvision GmbH
Organization:
Okuvision GmbH
Study Overview
Official Title:
Transcorneal Electrical Stimulation for the Treatment of Retinitis Pigmentosa - a Multicenter Safety Study of the Okustim System
Status:
COMPLETED
Status Verified Date:
2021-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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
Detailed 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 Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None