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Retinal Degeneration clinical trials

View clinical trials related to Retinal Degeneration.

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NCT ID: NCT03492853 Completed - Clinical trials for Peripheral Retinal Degenerations, Age Related Macular Degeneration Polymorphisms

The Association of the Peripheral Retinal Changes and Genotypic Changes in Patients With Age Related Macular Degeneration

Start date: January 1, 2015
Phase:
Study type: Observational [Patient Registry]

Purpose: To examine the genotypes associated with the peripheral retinal phenotypic features in patients with age-related macular degeneration documented with wide-field imaging. Design: Clinic-based case series study in Croatia. Participants: 160 patients >50 years of age known to have early or advanced AMD and 150 subjects >50 years of age without known AMD (controls) Methods: Both groups of patients were examined with ophthalmoscopy and OCT to confirm their classification. Posterior and peripheral fundus features were documented with Optos wide-field imaging (Optos P200MA, Optos Plc, Dunfermline, Scotland) and graded. DNA was extracted from blood samples and gene polymorphisms were evaluated for complement factor H (CFH) rs1061170 and rs1410996, age-related maculopathy susceptibility (ARMS2) rs10490924, high temperature requirement factor A1 (HtrA1) rs11200638, complement factor B (CFB) rs4151667 and rs641153, complement factor 2 (C2) rs9332739 and rs547154 and complement factor 3 (C3) rs2230199.

NCT ID: NCT03396042 Completed - Eye Diseases Clinical Trials

Natural History Study of CEP290-Related Retinal Degeneration

Start date: December 17, 2017
Phase:
Study type: Observational

A prospective natural history study with systematic assessments and uniform follow-up to provide a high-quality dataset for assisting in the design of future clinical treatment trials involving patients with CEP290-related retinal degeneration caused by the common intron 26 mutation.

NCT ID: NCT03321253 Completed - Retinal Detachment Clinical Trials

Changes of Macular Pigment and Parameters of Eyes After YAG Laser Treatment in Cases With Capsule Opacification

Start date: October 23, 2015
Phase: N/A
Study type: Interventional

It has been hypothesized that potential effects of laser Nd: YAG laser posterior capsulotomy may affect macular pigment as well as choroidal thickness, macular thickness and anterior chamber parameters, so it was aimed to investigate possible effects of Nd: YAG laser posterior capsulotomy on macular pigment optical density, choroidal thickness, macular thickness and anterior chamber parameters in cases with posterior capsule opacification in this study.

NCT ID: NCT03318549 Completed - Glaucoma Clinical Trials

BCI and Evaluation of Visual and Task Performance in Subjects With Eye Diseases

Start date: October 29, 2018
Phase: N/A
Study type: Interventional

The purpose of this research study is to better understand the impact of visual impairment caused by different eye diseases on the ability to perform daily activities and compare it to that in patients without eye diseases.

NCT ID: NCT03150654 Completed - Clinical trials for Diabetic Retinopathy

The Effect of Laser Treatment on Macular Pigment of Eye in Cases With Diabetes

Start date: October 1, 2015
Phase: N/A
Study type: Interventional

It has been hypothesized that thermal damage of laser pan-retinal photocoagulation may affect macular pigment as well as inner layer cells in the retina, so it was aimed to investigate possible effect of conventional laser pan-retinal photocoagulation on macular pigment optical density in diabetic retinopathy patients without macular edema and pathology in this study.

NCT ID: NCT03146078 Active, not recruiting - Clinical trials for Usher Syndrome, Type 2A

Rate of Progression in USH2A-related Retinal Degeneration

RUSH2A
Start date: August 11, 2017
Phase:
Study type: Observational

The overall goal of this project funded by the Foundation Fighting Blindness is to characterize the natural history of disease progression in patients with USH2A related retinal degeneration associated with congenital hearing loss (Usher syndrome type 2a) or non-syndromic retinitis pigmentosa (RP39).

NCT ID: NCT03078309 Recruiting - Clinical trials for Retinitis Pigmentosa

The Effects of Cannabis on Visual Functions in Healthy and Retinitis Pigmentosa Patients

Start date: September 1, 2018
Phase: Early Phase 1
Study type: Interventional

Medical Marijuana is used widely, and its effects on the visual system and the function of the retina have not been investigated thoroughly. Some evidence suggests that cannabinoids may be beneficial in certain degenerative diseases of the retina. The purpose of the study is 1. To determine whether cannabis derivatives affect the visual functions in healthy adults 2. To examine the effect of cannabis derivatives on the retina of retinitis pigmentosa patients

NCT ID: NCT03071055 Completed - Clinical trials for Exudative Age Related Macular Degeneration

Efficacy of Biweekly Ranibizumab (0.5 mg) for Exudative Macular Degeneration Retinal Edema Refractory to Anti-VEGF

Start date: October 1, 2017
Phase: Phase 2
Study type: Interventional

This is a 24 week open label study to assess the efficacy of bi-weekly ranibizumab for patients with retinal fluid due to exudative macular degeneration refractory to monthly therapy.

NCT ID: NCT02903576 Completed - Clinical trials for Age Related Macular Degeneration

Stem Cell Therapy for Outer Retinal Degenerations

Start date: August 2015
Phase: Phase 1/Phase 2
Study type: Interventional

This study is a Phase I/II , open label,non randomized, prospective study to determine the safety of human embryonic stem cell derived Retinal pigmented epithelium (hESC RPE) sub retinal injections versus hESC RPE seeded on a polymeric substrate implanted in the sub retinal space,

NCT ID: NCT02814435 Completed - Clinical trials for Retinal Degeneration

Quality of Life Measures in Patients With Retinal Degeneration

Start date: July 2016
Phase:
Study type: Observational

Inherited retinal degeneration (IRD) is a major cause of blindness and partial loss of vision cases in the UK and starts at an early age. The purpose of this observational study is to use the results of two questionnaires and a computerised test testing contrast sensitivity, to assess the impact of IRD on quality of life. This study will involve collecting data from patients with IRD, but also collecting data from normal controls.