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Glaucoma clinical trials

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NCT ID: NCT02524431 Withdrawn - Glaucoma Clinical Trials

The Changes Within the Cells of the Drainage System of the Eye in Patients With Glaucoma

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

The purpose of this study is to try to identify the cause of damage to the drainage system of the eye (the trabecular meshwork). Damage to this system may cause elevation in the pressure within the eye and thereby damage to the optic nerve and the vision.

NCT ID: NCT02438319 Withdrawn - Open Angle Glaucoma Clinical Trials

Automatic vs. Manual Optic Disc Planimetry

Planimetry
Start date: July 1, 2017
Phase:
Study type: Observational

Manually and automatically by mashing learning algorithm optic disc will be evaluated (planimetry).

NCT ID: NCT02031380 Withdrawn - Clinical trials for Glaucoma, Open-Angle [C11.525.381.407]

iDropper Usability in Glaucoma

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

The purpose of this study is to evaluate the usability of a medication management support system for glaucoma patients self-administering eye drops named iDropper. The iDropper system is a home-based ocular medication management system that reminds, instructs, dispenses, and records eye drop medication usage. The iDropper system will be evaluated among a cohort of glaucoma subjects self-administering eye drops for 4-weeks.

NCT ID: NCT01994564 Withdrawn - Open Angle Glaucoma Clinical Trials

Prevalence of Dyschromatopsia in Glaucoma Patients

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

Glaucoma is a progressive disease resulting in loss of retinal nerve cells and their axons (retinal nerve fibers). Retinal nerve fibers are ordered in a special manner when they enter the optic nerve. Hence, damage to the retinal nerve fibers by glaucoma results in visual field defects at certain locations. Furthermore, the retinal nerve fiber layers from different receptors for different colors are ordered in a special manner as well. Thus, it is possible that glaucomatous damage causes color vision dysfunction (dyschromatopsia). At the moment there is disagreement whether dyschromatopsia occurs at early- to mid-stage or only in end-stage glaucoma. By testing color vision in glaucoma patients the prevalence of dyschromatopsia in glaucoma and in different stages of the disease will be investigated.

NCT ID: NCT01927406 Withdrawn - Glaucoma Clinical Trials

The Secondary Beneficial Effects of Prostaglandin Analog Treatment in Thyroid Eye Disease Patients.

Start date: June 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the potential secondary beneficial effect of prostaglandin analogues (PA) treatment in thyroid eye disease (TED) patients. This study aims to determine if PA would change the course of the orbitopathy in TED patients by altering the progression of the common features of TED, including fatty hypertrophy, proptosis, eyelid retraction and optic nerve compression. The eyes with thyroid eye disease and elevated intraocular pressure will be randomised to the PA treatment and the other eye will serve as a control eye and will be treated with Timolol.

NCT ID: NCT01906151 Withdrawn - Glaucoma Clinical Trials

IOP Pattern in Primary Angle Closure and Primary Angle Closure Glaucoma Patients, Before and After LPI

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

The purpose of the study is to determine the relationship of the intraocular pressure patterns recorded during 2 sessions using Triggerfish, before and after elective laser peripheral iridotomy in angle closure glaucoma patients

NCT ID: NCT01766947 Withdrawn - Clinical trials for Primary Open Angle Glaucoma

IOP Fluctuations in Primary Open Angle Glaucoma Patients Before and After Deep Sclerectomy

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

Primary open angle glaucoma (POAG) is associated with inadequate drainage of the aqueous humor via the trabecular meshwork through the Schlemm's canal towards the systemic circulation. This may lead to an increase in IOP and may damage the optic nerve. The purpose of glaucoma management is to lower IOP in order to prevent progression of the optic neuropathy and subsequent visual loss. Firstline treatment usually includes IOP-lowering drug therapy. However, if IOP remains uncontrolled and/or the optic nerve damage progresses despite controlled IOP, surgery may be indicated. Deep sclerectomy (DS) is a non-penetrating surgical procedure for the treatment of open angle glaucoma that allows the enhancement of the aqueous outflow by removing part of the inner wall of Schlemm's canal and trabecular meshwork. DS was shown to achieve a good control on IOP over the long term. The purpose of this study is to assess the 24-hour IOP fluctuation profile recorded with Triggerfish in patients with POAG before and after DS.

NCT ID: NCT01726569 Withdrawn - Glaucoma Clinical Trials

Post-operative Satisfaction With Glaucoma Surgery Trial

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

1. Investigate degree of postoperative satisfaction in county level hospital glaucoma patients. 2. Investigate the effect of educational intervention affect the degree of satisfaction in glaucoma patients. 3. Investigate the effect factors of postoperative satisfaction.

NCT ID: NCT01721707 Withdrawn - Ocular Hypertension Clinical Trials

Latanoprost/Brinzolamide BID Versus Latanoprost BID in Patients With OAG or OH

Start date: December 2012
Phase: Phase 3
Study type: Interventional

This study is a double-masked, randomized, parallel group study in patients with open angle glaucoma or ocular hypertension. The aim of this study is to verify the efficacy of the fixed combination of Latanoprost 50 mcg / mL / brinzolamide 10mg/ml eye drops compared to Latanoprost 50μg/mL eye drops in reducing IOP

NCT ID: NCT01696383 Withdrawn - Glaucoma Clinical Trials

Assessing the Efficacy of DuoTrav as a Replacement Therapy in Glaucoma Patients in Russia

Start date: February 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy of changing to DuoTrav® (Travoprost 0.004%/Timolol 0.5%) from prior prostaglandin analogue or beta-blocker monotherapy in Russian glaucoma patients with open-angle glaucoma or ocular hypertension whose intraocular pressure (IOP) is uncontrolled while on their current treatment.