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Refractive Errors clinical trials

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NCT ID: NCT02710292 Completed - Refractive Error Clinical Trials

Clinical Evaluation of DAILIES TOTAL 1® Performance in a Japanese Population

Start date: April 25, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare DAILIES TOTAL1® (DT1) to 1-DAY ACUVUE® TruEye® (TE) for Investigator-rated successful lens centration in Japanese population.

NCT ID: NCT02699684 Completed - Refractive Error Clinical Trials

Comparison of Lotrafilcon B Lenses With Different Packaging Solutions

Start date: May 12, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate AIR OPTIX® plus HYDRAGLYDE® (AOHG) contact lenses compared to AIR OPTIX® AQUA (AOA) contact lenses in overall lens fit.

NCT ID: NCT02696317 Completed - Refractive Error Clinical Trials

Clinical Evaluation of ACUVUE® OASYS® 1-Day and ACUVUE® OASYS®

Start date: March 18, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the performance of two commercially-available silicone hydrogel contact lenses in normal and low humidity environments after at least 7 days of wear.

NCT ID: NCT02694835 Completed - Refractive Error Clinical Trials

Initial Performance of a Modified Daily Disposable Contact Lens

Start date: March 21, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the incidence of ocular discomfort device-related adverse events with DAILIES TOTAL1® with UV Absorber (DT1 UV) contact lenses compared with current DAILIES TOTAL1® (DT1) contact lenses.

NCT ID: NCT02687022 Not yet recruiting - Refractive Errors Clinical Trials

Measurement Repeatability in Contemporary Aberrometry

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

Wavefront scans are a common form of diagnostic test applied in preparing patients for laser eye surgery. An optical map of the eye is created by wavefront scanning, and information from these maps is used to program lasers used to correct focusing errors in the eye. Here the investigators are comparing how repeatable measurements are with a new wavefront scanner and one that is already in widespread use.

NCT ID: NCT02675751 Completed - Clinical trials for Stable Myopic Refractive Error, With or Without Astigmatism

Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced Wavescan Studio™ System and Star S4 IR™

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

Prospective, multicenter, bilaterally-treated, open-label, non-randomized clinical trial.

NCT ID: NCT02667509 Completed - Refractive Error Clinical Trials

The Evolutionary Model of Mild-to-moderate Myopia in China

Start date: January 2005
Phase: N/A
Study type: Observational

Myopia has emerged as a major health issue in east Asia, because of its increasingly high prevalence in the past few decades (now 80-90% in school-leavers), and because of the sight-threatening pathologies associated with high myopia, which now aff ects 10-20% of those completing secondary schooling in this part of the world. Similar, but less marked, changes are occurring in other parts of the world. The higher prevalence of myopia in east Asian cities seems to be associated with increasing educational pressures, combined with life-style changes, which have reduced the time children spend outside.

NCT ID: NCT02607384 Completed - Refractive Error Clinical Trials

The Baltimore Reading and Eye Disease Study

BREDS
Start date: November 2014
Phase: N/A
Study type: Interventional

The Baltimore Reading and Eye Disease Study (BREDS) is a two year study to determine the prevalence of vision problems in an early school age population with reading difficulty. Comprehensive vision and reading tests will be administered to 400 students at participating schools in the Baltimore City Public School system. A secondary goal is to examine the impact of vision treatment on reading performance. Children with refractive error or convergence insufficiency will be provided treatment free of charge. The investigators will evaluate the impact that the treatment has on vision function and reading performance.

NCT ID: NCT02553681 Completed - Ametropia Clinical Trials

Clinical Evaluation of HPT Treated Rigid Contact Lenses Made From Roflufocon D

Start date: July 2015
Phase: N/A
Study type: Interventional

This will be an up to six months, subject-masked, contralateral, parallel-group, randomised, daily wear study. All subjects will wear the Test lens in one eye and the Control lens in the other eye. Data from the first four weeks of Test and Control lens exposure will be used for the FDA 510 (k) submission.

NCT ID: NCT02528123 Completed - Myopia Clinical Trials

VisuMax Femtosecond Laser Small Incision Lenticule Extraction for the Correction of High Myopia

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

The purpose of this study is to validate the safety and effectiveness of treating myopia (short-sightedness) higher than -10D using small incision lenticule extraction (SMILE) with the VisuMax femtosecond laser.