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Glaucoma clinical trials

View clinical trials related to Glaucoma.

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NCT ID: NCT02622334 Completed - Glaucoma Clinical Trials

A Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RO5093151 in Patients With Primary Open Angle Glaucoma (POAG) or Ocular Hypertension (OHT).

Start date: December 29, 2015
Phase: Phase 1
Study type: Interventional

The purpose of the study is to assess the safety, tolerability, and IOP effects of RO5093151 following 7 days of topical ocular treatment in patients with primary open angle glaucoma or ocular hypertension.

NCT ID: NCT02622191 Completed - Glaucoma Clinical Trials

Analysis of the Eye in Patients With Primary Open-Angle Glaucoma and a Visual Field Defect in One Eye

Start date: November 2012
Phase: N/A
Study type: Interventional

The study aims to further understand glaucoma pathogenesis and progression by utilizing enhanced depth imaging optical coherence tomography to visualize and measure lamina cribrosa in vivo and segmentation technology to accurately delineate and measure boundaries of the retinal layers. Investigators will elaborate further on key concepts of lamina cribrosa thickness and trans-synaptic degeneration.

NCT ID: NCT02622178 Completed - Glaucoma Diagnosis Clinical Trials

How Accurately Does the Diopsys Visual Evoked Potential (VEP) Vision Testing System Detect Glaucoma?

Start date: September 2011
Phase: N/A
Study type: Interventional

Evaluate sensitivity and specificity of NOVA-DN visually evoked potentials (VEP) protocol and new software method (Corda) for glaucoma detection using optical coherence tomography (OCT) images to differentiate between normal subjects and glaucoma suspects.

NCT ID: NCT02617459 Completed - Ocular Hypertension Clinical Trials

Levobetaxolol Hydrochloride Eye Drops for Treatment of Primary Open-angle Glaucoma or Ocular Hypertension

Start date: January 4, 2019
Phase: Phase 3
Study type: Interventional

To evaluate the safety and efficacy of Levobetaxolol in Chinese patients with glaucoma.

NCT ID: NCT02614651 Completed - Glaucoma Clinical Trials

AUgmented REality for the Visually Impaired - Part 1

AUREVI 1
Start date: May 2016
Phase: N/A
Study type: Interventional

The main objective of this study is to quantify vision parameters in subjects with concentric visual field constriction, and this in relation to the display on virtual reality goggles. More specifically: - The maximum brightness value for visual comfort (THRESHOLD_MAX) - The minimum value of the perceptible light contrast in low light perceptible (THRESHOLD_MIN) - The speed of light change adaptation in the range [THRESHOLD_MAX-THRESHOLD_MIN] and [THRESHOLD_MIN-THRESHOLD_MAX].

NCT ID: NCT02613533 Completed - Glaucoma Clinical Trials

Water Drinking Test in Patients With Occludable Angle

Start date: February 2010
Phase: N/A
Study type: Interventional

The water drinking test (WDT), is a predictive test that has been used to detect primary open angle glaucoma and recently has been demonstrated as a predictor of the diurnal tension curve. Clinically accurate provocative tests for asymptomatic eyes with shallow anterior chambers and narrow angles are highly desirable to detect patients prone to angle closure glaucoma. The aim of this pilot study is to evaluate the possible role of water drinking test in patients with narrow angles who are scheduled for prophylactic laser iridotomy.

NCT ID: NCT02612571 Completed - Glaucoma Clinical Trials

Comparing Rates of Glaucoma in Professional Wind Versus Non-Wind Instrument Players

Start date: July 2015
Phase: N/A
Study type: Observational

The purpose of the present study is to compare rates of glaucomatous optic neuropathy in professional wind versus non-wind instrument players in the Philadelphia Orchestra. A secondary objective is to evaluate intra-ocular pressure and choroidal thickness of wind instrument players under variable playing conditions.

NCT ID: NCT02609204 Completed - Glaucoma Clinical Trials

Normative Database for Pattern Electroretinogram (PERG) and Flash Electroretinogram (FERG)

DIOPSYS-ND
Start date: November 2014
Phase: N/A
Study type: Interventional

The main goal of the study is to compile a normative database for the Neuro Optic Vision Assessment (NOVATM) Pattern Electroretinogram (PERG) and Flash Electroretinogram (FERG) modules. This normalization intends to be included in a probabilistic analysis protocol to allow NOVATM PERG/FERG users to identify patients with results outside the normal ranges.

NCT ID: NCT02604953 Completed - Glaucoma Clinical Trials

Comparing SD-tVEP and PERG Tests Between Patients With Glaucoma, Patients With High Eye Pressure and "Normal" Patients

Start date: July 2014
Phase: N/A
Study type: Observational

Wills Eye Hospital Glaucoma Research Center will conduct a 1-year prospective study to assess the ability of a Short Duration Transient Visual Evoked Potential (SD- tVEP) and a Steady-State Pattern electro-retinogram (PERG) vision testing system to detect visual dysfunction in patients with ocular hypertension. The study aims to assess the reversibility of retinal ganglion cell (RGC) dysfunction after administering intraocular pressure (IOP) lowering treatment. The investigators hypothesize that SD-tVEP and PERG testing will help develop better treatment for glaucoma patients by increasing understanding of the physiological relationship of IOP and RGC in glaucomatous injury.

NCT ID: NCT02600403 Completed - Glaucoma Clinical Trials

Are There Changes in the Nerve Fiber Layer (NFL) After Lowering of Eye Pressure?

Start date: October 2011
Phase:
Study type: Observational

The aim of this study was to evaluate structural and functional improvement after lowering intraocular pressure (IOP) in patients with glaucoma using Spectral Domain Optical Coherence Tomography (SD-OCT), Visual Field (VF) testing, and Visual Evoked Potential (VEP).