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Retinal Dystrophies clinical trials

View clinical trials related to Retinal Dystrophies.

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NCT ID: NCT02670980 Completed - Clinical trials for Retinitis Pigmentosa

Compensation for Blindness With the Intelligent Retinal Implant System (IRIS V2) in Patients With Retinal Dystrophy

IRIS 2
Start date: January 2016
Phase: N/A
Study type: Interventional

This study evaluates the safety and effectiveness of the Intelligent Retinal Implants System (IRIS V2). Blind patient suffering from Retinitis Pigmentosa, Cone Rod Dystrophy, or Choroideremia are implanted with an Intelligent Retinal Implant Systeme. All subjects undergo ophthalmological examinations in predefined intervals after implantation. Ophthalmological examinations include funduscopy, slit lamp examination and OCT. All adverse events are recorded and analyzed. Efficacy is measured using functional vision and visual function tests before and after implantation as well as with the system on and system off.

NCT ID: NCT02230228 Completed - Clinical trials for Age-related Macular Degeneration

Phase 1 Safety Study of ALK-001 in Healthy Volunteers

Start date: April 2014
Phase: Phase 1
Study type: Interventional

This protocol is a phase 1 clinical study to assess the safety and pharmacokinetics of ALK-001 in healthy volunteers. Please contact trials@alkeus.com for any questions.

NCT ID: NCT01876147 Completed - Clinical trials for Age-related Macular Degeneration

Visual and Functional Assessment in Low Vision Patients

Start date: August 2013
Phase:
Study type: Observational

Vision testing is a fundamental part of every optometry and ophthalmology assessment. Traditional vision testing charts are not able to measure vision below a certain level. Vision in this range is classified as counting fingers (CF), hand movements (HM) and light perception (LP). These measures are not very accurate or easily quantifiable. They are also poorly understood in terms of impact on quality of life. This study aims to assess new methods for measuring the vision of patients with very low vision.

NCT ID: NCT01864486 Completed - Clinical trials for Retinitis Pigmentosa

Restoring Vision With the Intelligent Retinal Implant System (IRIS V1)in Patients With Retinal Dystrophy

IRIS-1
Start date: April 2013
Phase: N/A
Study type: Interventional

This study evaluates the safety and effectiveness of the Intelligent Retinal Implants System (IRIS V1)

NCT ID: NCT01546181 Completed - Diabetes Clinical Trials

Retinal Imaging by Adaptive Optics in Healthy Eyes and During Retinal and General Diseases

iPhot
Start date: October 2010
Phase:
Study type: Observational

Using an adaptive optics imaging device, retinal structures are observed in healthy and diseased subjects.

NCT ID: NCT01496040 Completed - Clinical trials for Leber Congenital Amaurosis

Clinical Gene Therapy Protocol for the Treatment of Retinal Dystrophy Caused by Defects in RPE65

RPE65
Start date: September 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is to assess the safety and efficacy of the active substance rAAV-2/4.hRPE65 in patients with Leber Congenital Amaurosis or Congenital severe early-onset retinal degeneration associated with RPE65 mutation.

NCT ID: NCT00422721 Completed - Retinal Diseases Clinical Trials

Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy

Start date: April 2007
Phase: N/A
Study type: Interventional

Retinal dystrophies are responsible for numerous cases of blindness, and there are no therapeutic possibilities today. Gene therapy is efficient in a dog model concerning dystrophy linked to a mutation of the rpe65 gene. If such a therapy is to be considered for humans, it is urgent to select, at a national level, patients suffering from dystrophy linked to a mutation of the rpe65 gene. The systematic correlation of phenotype/genotype is an anatomical-functional approach, but it also identifies patients who may be potentially included in a future gene therapy study. Indeed, identification of people with a mutation of rpe65 is still insufficient in France (compared to other European countries) because of a lack of systemic genotyping of retinal dystrophy.