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Astigmatism clinical trials

View clinical trials related to Astigmatism.

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NCT ID: NCT03082599 Completed - Clinical trials for Astigmatism Bilateral

Symfony Toric Intraocular Lens Visual Outcomes

Start date: February 17, 2017
Phase: N/A
Study type: Interventional

In July 2016, the FDA approved an extended depth of focus (EDOF) IOL (Tecnis Symfony, Abbott Medical Optics) helping to improve the sharpness of vision at near, intermediate and far distances reducing the need of glasses after cataract surgery. It is available in both a non-toric version and a toric version for patients with astigmatism. The difference between this lens and the multifocal (MIOL) counterpart is that the EDOF, similarly to a monofocal IOL, has one focal point (elongated in the EDOF) while the multifocals have 2 focal points; therefore, having less of a halo and glare problem. Pivotal trial results where Symfony was compared to a monofocal IOL showed similar uncorrected distance visual acuity (UCDVA), better intermediate (77% vs. 34% 20/25 uncorrected intermediate visual acuity - UCIVA) and near vision (Symfony patients were able to read two additional, progressively smaller lines compared to the monofocal IOL).A One potential disadvantage of the EDOF IOL compared to a MIOL is the visual performance at near.B One option to deal with this potential shortcoming is to set the non-dominant eye for a small residual myopic error (-0.50 D)C what is referred to as nano-vision or mini mono-vision.

NCT ID: NCT03063164 Completed - Myopia Clinical Trials

A Comparison of LASIK Outcomes Using Two Femtosecond Lasers

Start date: February 14, 2017
Phase: N/A
Study type: Interventional

Comparing LASIK outcomes using two femtosecond lasers

NCT ID: NCT03054649 Completed - Cataract Clinical Trials

ClarVista HARMONI Toric Trial With Intraoperative Exchange

Start date: June 28, 2016
Phase: N/A
Study type: Interventional

The purpose of this study was to demonstrate the safety and effectiveness of the HARMONI® Modular Intraocular Lens System with a toric optic in subjects with pre-existing corneal astigmatism in need of cataract surgery.

NCT ID: NCT03050697 Completed - Cataract Clinical Trials

Evaluation of the Safety and Performance of the HARMONI® Toric Lens

Start date: September 28, 2016
Phase: N/A
Study type: Interventional

The purpose of this study was to evaluate the safety and effectiveness of the HARMONI® Modular Intraocular Lens System with a toric optic (HMTIOL) in subjects with pre-existing corneal astigmatism in need of cataract surgery.

NCT ID: NCT03006458 Completed - Astigmatism Clinical Trials

A Clinical Comparison of 2 Multifocal Toric XR (Extended Range) Contact Lenses

Start date: December 2016
Phase: N/A
Study type: Interventional

This study aims to compare the clinical performance and subjective acceptance of the comfilcon A and the omafilcon B soft contact lenses.

NCT ID: NCT02950545 Completed - Astigmatism Clinical Trials

Evaluating and Improving Functional Driving Vision of Patients With Astigmatism: Phase 3

Start date: April 2016
Phase: N/A
Study type: Interventional

It is a common clinical practice to leave small amounts of astigmatism uncorrected in contact lens wearers. Therefore, some drivers who have astigmatism and wear contact lenses may experience blur while driving. The purpose of this study is to determine if correcting small amounts of astigmatism with contact lenses will improve driving safety.

NCT ID: NCT02939001 Completed - Cataract Clinical Trials

Evaluating the Effect of Laser Vision Surgery, Phakic Intraocular Lens Implantation, Cataract Surgery, and Pupil Dilation on the Iris Recognition Scanner Function of Smartphone

Start date: October 3, 2016
Phase: N/A
Study type: Interventional

This study included patients who visit for refractive surgery (photorefractive keratectomy, photorefractive keratectomy with with corneal collagen cross linking, laser in situ keratomileusis, small incision lenticule extraction), phakic Intraocular Lens implantation (Implantable Collamer Lens, artiflex), and cataract surgery. Patients will be examined whether iris recognition scanner of smartphone works before and after surgery. In addition, before and after pupil dilation (5mm, 6mm, 7mm, 8mm), patients will be examined whether iris recognition scanner of smartphone works well.

NCT ID: NCT02921412 Completed - Astigmatism Clinical Trials

Performance of Fanfilcon A Toric Lenses After at Least One Month Wearing Enfilcon A Toric Lenses

Start date: October 1, 2016
Phase: N/A
Study type: Interventional

This is a prospective, multi-center, subject-masked, bilateral, daily wear, two-month dispensing study

NCT ID: NCT02847169 Completed - Astigmatism Clinical Trials

Clinical Performance of Toric Hydrogel Contact Lenses Following One Week of Daily Wear

Start date: September 2016
Phase: N/A
Study type: Interventional

The aim of this prospective study is to evaluate the clinical performance of filcon IV1 toric and ocufilcon D toric contact lenses after 1 week of wear in each pair.

NCT ID: NCT02801006 Completed - Astigmatism Clinical Trials

The Clinical Study of Silicone Hydrogel Daily Disposable Stenfilcon A Toric Lens

Start date: April 2016
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the clinical performance of stenfilcon A toric lenses compared with etafilcon A toric lenses for astigmatism. If it is valuable, the clinical performance of stenfilcon A toric lens is also evaluated compared with habitual lenses.