Clinical Trials Logo

Visual Acuity clinical trials

View clinical trials related to Visual Acuity.

Filter by:

NCT ID: NCT01926704 Completed - Visual Acuity Clinical Trials

MTF Image Modifications

Start date: October 2013
Phase: N/A
Study type: Observational

Human visual acuity and contrast sensitivity are highly dependent on various different parameters. Each should be optimized for perfect visual performance. However, in real life our eyes lack such parameters, which might lead to unsatisfying results even after spectacle correction or contact lenses. A promising approach would be to design intra ocular lenses (IOL), which are implanted into the eye for example in the course of cataract extraction and are able to compensate for the human eyes' aberrations. For example cutoff frequency, edge-sharpness or specific contrast for selected structure sizes would need to be considered. Since, an aberration free optical system is almost impossible and since the impact of each single parameter is not yet known, IOL design parameters would have to be chosen very carefully. Furthermore, image quality of IOLs still is tested ex vivo by ray tracing for example, but this does not guarantee perfect function after implantation, as our visual system has complex image precessing units form the retina to the brain. The present study picks one of these parameters and seeks to assess its impact on visual quality in-vivo. By subjectively grading different images with objective changes to image quality by variations of the modulation transfer function (MTF), the potential influence and thus on our subjective visual impression shall be assessed.

NCT ID: NCT01873781 Completed - Visual Acuity Clinical Trials

A Pilot Study Simulating Multifocal Intraocular Lenses in Healthy Subjects

Start date: April 2013
Phase: N/A
Study type: Observational

Age related cataracts are responsible for about 51 percent of blindness worldwide and according to the WHO affect about 20 million people, according to the WH . As cataract surgery is firstline treatment in the western world, there is a constant attempt to improve artificial intraocular lenes (IOL). As for this study, the investigators seek to compare four different IOL designs in in a psychophysiological setting, allowing to assess the impact of these IOLs on vision and psychological processing of visual information. As these IOLs also have downsides, such as reduced light intensity or image alterations, the subjective preference and overall impression shall be investigated. The healthy subjects look through a stable spectacle frame mounted onto a table, which enables the investigator to insert the different IOLs. This would allow subjective testing of IOLs before surgery.

NCT ID: NCT01219478 Completed - Visual Acuity Clinical Trials

Research of the Correlation Between Metabolic Syndrome, Retinal Thickness and Visual Acuity

Start date: January 2009
Phase: N/A
Study type: Observational

Purpose: To investigate the relationship between retinal thickness (RT) and metabolic risks (MRs) in patients without retinal lesion. Methods: Fifty-two patients over 60 y/o were divided into four groups according to their MRs of hypertension, hyperlipidemia or hyperglyceremia. After complete ophthalmic examination, optical coherence tomography was performed to measure RT.

NCT ID: NCT01191502 Completed - Visual Acuity Clinical Trials

Comparative Study of Photopic and Mesopic Distance, Intermediate and Near Visual Acuity, and Spectacle Independence

Start date: January 2010
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate visual acuity in different lighting conditions (daylight and night time) and distances (distance, near and intermediate), and the independence of glasses, in patients who have had binocular implantation of the Tecnis Multifocal IOL or the Crystalens™ HD Accommodating IOL.

NCT ID: NCT01069029 Completed - Visual Acuity Clinical Trials

Combined Versus Successive Macular Hole and Cataract Surgery

Start date: January 2006
Phase: N/A
Study type: Observational

The purpose of this study is to compare functional and anatomical results of a combined surgery and two time surgery for macular hole and cataract extraction in one hundred and twenty patients (120 eyes) with idiopathic Macular Hole (MH) and cataract in two academic centers.

NCT ID: NCT00999284 Completed - Visual Acuity Clinical Trials

Ophthalmologic Examinations After Infusion of ZK200775

Start date: December 1996
Phase: Phase 1
Study type: Interventional

ZK 200775 is an antagonist at the α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) receptor and had earned attention a possible neuroprotective agent in cerebral ischemia. Probands receiving the agent within a stroke therapy related Phase I trial reported on an alteration of visual perception. In this trial, the effects of ZK 200775 on the visual system will be analyzed in detail. In a randomised, placebo-controlled, double-blind study eyes and vision will be examined before and after the intravenous administration of ZK 200775. The following methods will be applied: clinical examination, visual acuity, ophthalmoscopy, colour vision, rod absolute threshold, central visual field, pattern-reversal visual evoked potentials (pVEP), ON-OFF and full-field electroretinogram (ERG).

NCT ID: NCT00870597 Completed - Visual Acuity Clinical Trials

Transconjunctival Sutureless 25-Gauge Vitrectomy

TSV-25G
Start date: January 2007
Phase: Phase 3
Study type: Interventional

The aim of this study was to evaluate the role of 25-gauge transconjuntival sutureless vitrectomy (TSV) in patients with persistent vitreous floaters who underwent multifocal intraocular lens (IOL) implantation.

NCT ID: NCT00813891 Not yet recruiting - Clinical trials for Macular Degeneration

Efficacy of Ranibizumab in Combination With Photodynamic Therapy for Wet Age-Related Macular Degeneration

Start date: January 2009
Phase: Phase 4
Study type: Interventional

The purpose of the investigators study is to look at the visual outcomes of Ranibizumab injections in combination with photodynamic therapy for the treatment of neovascular age-related macular degeneration.

NCT ID: NCT00800423 Not yet recruiting - Visual Acuity Clinical Trials

Effect of Topical Brimonidine on Post Cataract Surgery Corneal Edema

Start date: January 2009
Phase: Phase 3
Study type: Interventional

Most patients undergoing cataract surgery suffer from corneal edema after the surgery. Brimonidine drops are a well known and safe Anti-glaucoma medication. the investigators have made several clinical observations that patients receiving Brimonidine drops had a faster resolution of their corneal edema even if they had normal intra-ocular pressure. The investigators believe that administering topical Brimonidine to patients with significant post operative corneal edema will hasten the resolution of their corneal edema.

NCT ID: NCT00759096 Completed - Visual Acuity Clinical Trials

Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL

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

The purpose of this study is to assess uniocular and binocular unaided distance, intermediate, and near VA; contrast sensitivity, accommodation amplitude, stereopsis, glare testing, ocular aberrations and the clinical satisfaction assessment after bilateral implant of the Restor IOL.