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Glaucoma clinical trials

View clinical trials related to Glaucoma.

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NCT ID: NCT02628327 Completed - Glaucoma Clinical Trials

Factors Influencing Patient Satisfaction in a Glaucoma Population

FIPSS
Start date: June 2015
Phase: N/A
Study type: Observational

1. To administer a questionnaire to patients seen by Wills Eye Glaucoma Department physicians at Wills Eye Hospital assessing satisfaction with their office visit, vision related quality of life, and related issues. 2. To collect and de-identify information from each participant's medical chart related to their care including information pertaining to demographics, disease severity, and prior and current treatment 3. To assess the correlations between demographic factors, vision related quality of life, eye disease, and treatments with patient satisfaction survey responses.

NCT ID: NCT02628223 Completed - Glaucoma Clinical Trials

180 Degree vs. 360 Degree Selective Laser Trabeculoplasty as Initial Therapy for Glaucoma

Start date: September 2014
Phase: N/A
Study type: Interventional

Selective laser trabeculoplasty (SLT) is a well-recognized way to lower eye pressure in treatment of glaucoma. This treatment is performed for 180 degrees or 360 degrees, and studies at academic centers have shown mixed results when comparing the success rates of 180 degrees or 360 degrees. Both protocols are now typically done by comprehensive ophthalmologists. However, there is no data that compares success rates of 180 degrees and 360 degrees in the community setting.

NCT ID: NCT02627352 Completed - Glaucoma Clinical Trials

How Safe and Effective is Micropulse Transscleral Cyclophotocoagulation in Patients With Uncontrolled Glaucoma?

TSCPC
Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the surgical outcomes of the micropulse transscleral cyclophotocoagulation (mTSCPC) in patients with uncontrolled glaucoma; analyze intraocular pressure lowering effect; and correlate related treatment parameters pending enrollment of sufficient numbers of dark pigmented versus light pigmented eyes.

NCT ID: NCT02627339 Completed - Glaucoma Clinical Trials

Building a Database of Results From People Without Eye Problems

SPARCS
Start date: August 2012
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to build a database of results from a new test that measures contrast sensitivity (the Spaeth-Richman Contrast Sensitivity Test (SPARCS)). Contrast sensitivity is an important part of your ability to see. When contrast sensitivity decreases, you are less able to see objects and detect motion. For instance, if you have decreased contrast sensitivity, you might be less able to read, see in the dark, drive, hit a ball, or walk safely. Decrease in contrast sensitivity leads to a decrease in quality of life.

NCT ID: NCT02624427 Completed - Glaucoma Clinical Trials

Goldmann Applanation Tonometry, Dynamic Contour Tonometry, and Corvis ST Tonometer

Start date: December 2015
Phase: N/A
Study type: Interventional

The study is investigating Intra ocular pressure (IOP) by Goldmann Applanation Tonometry, Dynamic Contour Tonometry, and the Corvis ST tonometer.

NCT ID: NCT02623738 Completed - Ocular Hypertension Clinical Trials

A Study Assessing the Efficacy and Safety of DE-117 Ophthalmic Solution in Subjects With Primary Open Angle Glaucoma or Ocular Hypertension -AYAME Study-

Start date: December 6, 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The purposes of this study are to determine the optimal concentration of DE-117 ophthalmic solution compared to the placebo ophthalmic solution and to determine if intraocular pressure reduction after 4 weeks of treatment with DE-117 ophthalmic solution is non-inferior to latanoprost ophthalmic solution 0.005%.

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.