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Astigmatism clinical trials

View clinical trials related to Astigmatism.

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NCT ID: NCT00584220 Completed - Astigmatism Clinical Trials

Evaluation of Two Toric Soft Contact Lenses After Two Weeks of Wear

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

The purpose of this study is to determine the relative performance of a new toric soft contact lens against a toric contact lens currently available in market, specifically with regards to the comfort and vision after two weeks of use.

NCT ID: NCT00583908 Completed - Astigmatism Clinical Trials

Evaluation of Orientation and Visual Acuity of Four Toric Soft Contact Lenses When Head is Tilted at 90 Degrees

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

The purpose of this study is to determine the relative performance of a new toric soft contact lens against three toric contact lens currently available in market, specifically with orientation and visual acuity when head is tilted at 90 degrees.

NCT ID: NCT00581659 Completed - Astigmatism Clinical Trials

Evaluation of the Bausch & Lomb PureVision Under Nighttime Driving Conditions

Start date: November 2007
Phase: N/A
Study type: Observational

The objective of this study is to quantify differences in nighttime driving performance between the Bausch & Lomb PureVision™ aspheric contact lenses and a conventional spherical contact lens. The primary aims of this study are to determine the differences between B&L PureVision™ aspheric contact lenses and a conventional spherical contact lens in visual performance measures associated with driving, such as number of objects seen. The secondary aims of this study are to determine differences between B&L PureVision™ aspheric contact lenses and a conventional spherical contact lens in driving performance measures such as number of objects hit.

NCT ID: NCT00542581 Completed - Cataracts Clinical Trials

Acrysof Toric SN60T3corneal Astigmatism Between 0.75 and 1.00 D.

TORILIOL
Start date: October 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the visual outcomes and patient satisfaction after implantation of a toric IOL in patients with predicted residual corneal astigmatism between 0.75 and 1.00 D. Cataract is prevalent throughout the world and IOLs are routinely implanted after the extraction of the cataractous lens. It is the most frequently performed surgery in the United States with an estimated 2-3 million procedures performed annually. With the aging population on the rise, as well as the increasing popularity of refractive intraocular lenses, the number of intraocular surgeries continues to rise. Over the years, the surgical technique has evolved from intracapsular extraction to modern phacoemulsification. This development has helped with the evolution of IOLs as well. The IOLs have advanced extensively: different materials and designs are available, permitting implantation through smaller, sutureless incisions. Traditional IOLs are of monofocal design providing vision at one distance, typically far; and correct mainly the spherical component of the refractive error. However, there are patients with corneal astigmatism that require additional surgical treatment such as laser correction (laser in situ leratomileusis, LASIK; photorefractive keratectomy, PRK) or limbal relaxing incisions, RLI). Another alternative is the use of a toric IOL, which has been especially designed to correct both the sphere and the astigmatism. The ACRYSOF Toric IOL is intended for primary implantation in the capsular bag of the eye for visual correction of aphakia and preexisting comeal astigmatism in adult patients with or without presbyopia, who desire improved uncorrected distance vision, reduction of residual refractive cylinder and increased spectacle independence for distance vision. The treatment selection of the corneal astigmatism depends on the amount of cylinder as follows, between 0.25 and 0.75 D creating the surgical incision on the steep axis; between 0.75 and 1.75 D, RLI; between 1 and 2.25 D, toric IOLs; and between 1 and 3.00 D, LASIK/PRK.

NCT ID: NCT00521833 Completed - Clinical trials for Surrgical Induced Astigmatism

Surgically Induced Astigmatism of Temporal Versus Nasal Clear Corneal Phacoemulsification

Start date: June 2005
Phase: N/A
Study type: Interventional

To compare the short-term astigmatic outcomes of phacoemulsification cataract surgery and intraocular lens implantation using temporal versus nasal clear corneal incisions.

NCT ID: NCT00366769 Completed - Myopia Clinical Trials

Evaluation of Outcomes Following LASIK Surgery Using CustomVue

Start date: September 2005
Phase: N/A
Study type: Interventional

The aim of the study was to evaluate visual outcomes, contrast sensitivity, glare and induced high order aberrations induced by the new CustomVue software use for wavefront-guided LASIK.

NCT ID: NCT00366743 Completed - Myopia Clinical Trials

Evaluation of Visual Outcomes After Myopic LASIK

Start date: May 2003
Phase: N/A
Study type: Interventional

The aim of the study was to evaluate visual outcomes, contrast sensitivity, glare testing and high order aberrations induced by different laser technologies and to evaluate differences in aberrometer technology. We hypothesized that there will not be differences among conventional or wavefront guided treatments.

NCT ID: NCT00366574 Completed - Myopia Clinical Trials

Comparison of a Laser Keratome to a Mechanical Microkeratome

Start date: September 2004
Phase: N/A
Study type: Interventional

The purpose of this study was to evaluate the performance of the INTRALASE®, a laser keratome which creates a corneal flap, and compare it to a mechanical microkeratome (Amadeus™). Our hypothesis is that there is no difference between the 2 devices.

NCT ID: NCT00365677 Completed - Myopia Clinical Trials

A Study to Investigate the Safety and Effectiveness of Aspheric Laser Refractive Surgery Treatments for Myopia

Start date: October 2005
Phase: N/A
Study type: Interventional

The objective of this study was to compare the safety and effectiveness of two versions of the Bausch & Lomb Zyoptix Tissue Saving Aspheric Algorithm versus the current Zyoptix Tissue Saving Algorithm when used for myopia and myopic astigmatism LASIK treatment.

NCT ID: NCT00365040 Completed - Refractive Errors Clinical Trials

Customized PRK With Mitomycin Versus Customized Lasik for Myopic Astigmatism

Start date: December 2004
Phase: N/A
Study type: Interventional

The present study was designed to compare the use of mitomycin in PRK for the treatment of refractive errors and to compare these results to customized Lasik