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Refractive Errors clinical trials

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NCT ID: NCT04955379 Recruiting - Refractive Errors Clinical Trials

Study in Pediatric Volunteers of a Handheld Device Versus a Standard Diagnostic Device in Ophthalmic Refraction

Start date: December 15, 2021
Phase: N/A
Study type: Interventional

This study is exploratory and examines whether the refraction results obtained from a novel optical device yields results similar to the ophthalmic refraction measurements obtained from an autorefractor in children.

NCT ID: NCT04942925 Completed - Myopia Clinical Trials

Clinical Comparison of Two Daily Disposable Contact Lenses - Pilot Study 3

Start date: July 20, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the overall performance of PRECISION1™ contact lenses when compared to INFUSE™ contact lenses.

NCT ID: NCT04908488 Completed - Astigmatism Clinical Trials

Clinical Performance of Two Daily Disposable Toric Soft Contact Lenses

Start date: July 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the clinical performance of PRECISION1™ for Astigmatism (P1fA) contact lenses with 1-DAY ACUVUE MOIST® for ASTIGMATISM (AMfA) contact lenses.

NCT ID: NCT04865354 Completed - Refractive Errors Clinical Trials

Clinical Comparison of Two Daily Disposable Contact Lenses

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

The purpose of this study is to compare the clinical performance of PRECISION1™ contact lenses to Clariti® 1 day contact lenses.

NCT ID: NCT04827511 Completed - Child, Only Clinical Trials

Refractive Disorders and Seric Vitamin D Level in Children With Disabilities

REDIC
Start date: January 1, 2019
Phase:
Study type: Observational [Patient Registry]

The investigator want to determine the refractive status of 80 children with disabilities and of 81 healthy children from a witness group. The vitamin D level of the children will be dosed for making different correlations with visual acuity status.

NCT ID: NCT04816266 Not yet recruiting - Error, Refractive Clinical Trials

Comparative Study in Measuring Anterior Chamber Depth

Start date: April 1, 2021
Phase:
Study type: Observational

Measuring parameters of anterior segment of the eye accurately is important for diagnosing variety of diseases and for cataract surgeries, glaucoma, refractive surgeries and post-operative follow-up. One of the anterior segment parameters is the anterior chamber depth. The anterior chamber depth (ACD) measurement provides valuable information in different fields in ophthalmology. Firstly, it is important for the new theoretical biometric formulas used to calculate the power of intraocular lenses (IOLs) .Secondly, phakic IOL implantation requires precise ACD measurement for both surgical planning and IOL power calculation. Thirdly, the ACD is also implicated as a screening risk factor for glaucoma. Additionally, precise ACD measurement is thought to be important to the accurate determination of the optic zone ablation diameter for keratorefractive surgery, as well as for the analysis of postoperative ACD changes. Different technologies are used in measurement of the anterior chamber depth Such as pentacam and iol maste

NCT ID: NCT04793893 Enrolling by invitation - Refractive Errors Clinical Trials

Treatment of Residual Hypermetropic Refraction on Young Patients After LASIK Using Human Fresh Corneal Lenticule Implantation With ReLEX Smile Surgery

Relex-Smile
Start date: January 8, 2019
Phase: N/A
Study type: Interventional

LASIK (laser-assisted in situ keratomileusis) is a type of refractive surgery for correction of myopia, hyperopia and astigmatism. Yet approximately 30% of operated patients have symptoms like glare, halos, dry eyes and especially residual hypermetrop refractive errors. Residual hypermetrop refractive errors are difficult to treat surgically, the current treatment is Refractive Lens Implantation - risks are similar to those of cataract surgery (endophthalmitis, loss of accommodation, etc.)

NCT ID: NCT04789382 Completed - Refractive Errors Clinical Trials

Three Daily Wear Monthly Replacement Silicone Hydrogel Contact Lenses With Two Multi-purpose Disinfecting Solution Combinations

Start date: April 7, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate corneal staining observed after 2 hours of wear with an investigational contact lens against both PureVision contact lenses pre-cycled with Biotrue and Biofinity contact lenses pre-cycled with RepleniSH.

NCT ID: NCT04783909 Completed - Cataract Clinical Trials

Refractive Outcomes After Cataract Surgery in Eyes With Pseudoexfoliation Syndrome

Start date: October 1, 2016
Phase:
Study type: Observational

To evaluate the refractive outcomes of cataract surgery in PEX syndrome and determine which of the commonly used IOL formulas (SRK/T, Barrett Universal II and Hill-RBF) is the best in predicting postoperative refractive outcomes in PEX.

NCT ID: NCT04756596 Recruiting - Refractive Errors Clinical Trials

A Web-based Digital Distance Visual Acuity Test

DDVIT
Start date: February 1, 2021
Phase:
Study type: Observational [Patient Registry]

Primary objective of this study is the development and validation of a web-based application for the examination of the distance visual acuity of normal- and low-vision patients.