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Astigmatism clinical trials

View clinical trials related to Astigmatism.

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NCT ID: NCT04676451 Completed - Cataract Clinical Trials

Femtosecond Laser Assisted Keratotomies for the Management of Corneal Astigmatism

Start date: May 14, 2018
Phase: N/A
Study type: Interventional

A cataract is a clouding of the lens that occurs naturally with age. Cataract surgery involves removal of the cloudy lens and replacement with an artificial one. A special laser (femtosecond laser) is now being used to help make cataract surgery safer and more accurate . The femtosecond laser can also be used to correct astigmatism, an irregular curvature of the cornea, at the time of cataract surgery through a procedure called astigmatic keratotomy (AK). This study is gathering information about the specific laser settings that are used to perform astigmatic keratotomies (AK) during cataract surgery. This information will be used to improve the outcomes of patients that receive cataract surgery with astigmatic keratotomies in the future.

NCT ID: NCT04652037 Completed - Cataract Clinical Trials

Visual Results of the Acrysof IQ Vivity Toric Extended Vision Intraocular Lens

Start date: March 17, 2021
Phase: N/A
Study type: Interventional

The main goal of this study is to evaluate real-world visual outcomes, rotational stability, and patient reported visual disturbances with a non-diffractive extended vision presbyopia and astigmatism correcting intraocular lens in patients with significant corneal astigmatism undergoing bilateral cataract surgery. This is important to ensure optimal results for patients who wish to have intraocular lenses that correct presbyopia and astigmatism, thus giving them a greater independence from spectacles and a better quality of life.

NCT ID: NCT04613882 Completed - Astigmatism Clinical Trials

Quantification of the Visual Benefits of Soft Toric Contact Lenses Compared to Soft Spherical Contact Lenses

Start date: September 28, 2021
Phase: N/A
Study type: Interventional

The aim of this work is to undertake a range of vision-related measures with soft toric contact lenses soft spherical contact lenses and spectacle lens correction across a range of levels of astigmatism.

NCT ID: NCT04542525 Completed - Aphakia Clinical Trials

Clinical Investigation of an AcrySof IQ PanOptix Toric Intraocular Lens

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness and safety of the TFNT20 low cylinder power intraocular lens when implanted in the eye to replace the natural lens following cataract removal.

NCT ID: NCT04536571 Completed - Myopia Clinical Trials

Vision Stability and Preference for Soft Toric vs. Soft Spherical Contact Lenses

Start date: September 3, 2020
Phase: N/A
Study type: Interventional

The principal hypothesis is to be tested in this work is that vision stability (the primary outcome measure) with a spherical contact lens correction vs. a toric contact lens correction will be the same.

NCT ID: NCT04528069 Completed - Aphakia Clinical Trials

Clinical Investigation of the Visual Outcomes and Safety of a Trifocal Toric IOL in an Asian Population

Start date: November 16, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the clinical performance of the ACRYSOF® IQ PanOptix® Toric Trifocal intraocular lens (IOL) when implanted in the eye following cataract removal in an Asian population.

NCT ID: NCT04475900 Completed - Glaucoma Clinical Trials

Computer-aided Diagnosis of Ocular Diseases Based on Corneal Biomechanics

EyeTwin
Start date: July 9, 2020
Phase:
Study type: Observational

The purpose of this study is the investigation of biomechanical properties of the cornea using computer-aided data analysis. Currently, it is known that keratoconus and glaucoma are ocular disease that are associated with biomechanical alterations of the cornea. Corneal ectasia, especially keratoconus, is a corneal disease that leads to an irreversible loss of visual acuity while the cornea becomes steeper, thinner and irregular. For these patients, surgical intervention (e.g. corneal cross-linking) is performed, in case of disease progression. In glaucoma, the information about corneal alterations serves in two ways, first, correct measurement of intra ocular pressure (IOP); second, early diagnosis of suspects before visual field defects are detectable. Especially, the Corvis ST is an air-puff tonometer that measures intraocular pressure, corneal thickness (CCT) as well as dynamic corneal response (DCR) parameters. Most of the DCR parameters are affected by IOP and CCT: Therefore, algorithm are needed to determine parameters without impact of IOP and CCT that are describe the biomechanical properties of the cornea.

NCT ID: NCT04468022 Completed - Hyperopia Clinical Trials

Toric Trifocal IOL Treatment With High Astigmatism and Hyperopia vs SMILE Enhancement After Trifocal IOL Treatment

Start date: June 1, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to assess visual and refractive outcomes after Toric Trifocal lens implantation and visual outcomes after laser vision correction (LVC) - ReLex Smile to correct residual refraction after 6 months of Toric Trifocal (IOL) implantation.

NCT ID: NCT04464044 Completed - Astigmatism Clinical Trials

Clinical Performance of a Daily Disposable Toric Silicone Hydrogel Contact Lens

Start date: July 20, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to obtain on-eye clinical performance data to evaluate the stability of axis orientation of DDT2 toric contact lenses in the intended population.

NCT ID: NCT04432181 Completed - Amblyopia Clinical Trials

Comparison of Deviation Types Among Astigmatic Children With Or Without Amblyopia

Start date: September 4, 2018
Phase:
Study type: Observational [Patient Registry]

the records of astigmatic children were reviewed and any deviation was investigated at near and distance. refractive errors, stereopsis, convergence insufficiency were also evaluated. children were divided into two groups according to the presence of amblyopia and ocular deviations and other parameters were compared between groups.