NCT01497379

Safety & Efficacy of Subretinal Implants for Partial Restoration of Vision in Blind Patients

Safety & Efficacy of Subretinal Implants for Partial Restoration of Vision in Blind Patients: A Prospective Mono- & Multicenter Clinical Study Based on Randomized Intra-individual Implant Activation in Degenerative Retinal Disease Patients.

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 2 (actual)
• Sponsor: Retina Implant AG · Industry
• Sex: All
• Age: 18 Years – 78 Years
• Healthy volunteers: Not accepted

Summary

Patients who are legally blind, caused by retinal degeneration of photoreceptor rods \& cones (e.g. Retinitis pigmentosa), receive a subretinal implant to restore vision partially.

Conditions

• Retinal Degeneration
• Retinitis Pigmentosa

Interventions

Type	Name	Description
PROCEDURE	surgical implantation of subretinal device	surgical implantation of subretinal device
PROCEDURE	surgical implantation of subretinal device	intra-individual implant OFF

Timeline

• Start date: 2011-10-01
• Primary completion: 2014-01-01
• Completion: 2015-01-01
• First posted: 2011-12-22
• Last updated: 2017-03-29

Locations

1 site across 1 country: Hong Kong