Clinical Trials Logo

Myopia clinical trials

View clinical trials related to Myopia.

Filter by:

NCT ID: NCT02196766 Completed - Myopia Clinical Trials

BIOCLEAN FIRST CARE EX in Combination With Biofinity Lens

Start date: July 2014
Phase: N/A
Study type: Interventional

To determine if patients are unreactive to the lens care solution / Biofinity combination.

NCT ID: NCT02193178 Completed - Myopia Clinical Trials

Multicenter Dispensing Study of Biofinity Toric Made-To-Order Lenses in Extended Power Ranges

Start date: July 2014
Phase: N/A
Study type: Interventional

The study hypothesis is that the Biofinity Toric XR lenses will perform as well as or better than the participants' habitual contact lenses.

NCT ID: NCT02186184 Completed - Myopia Clinical Trials

Effect of Orthokeratology Versus Spectacles on Myopia Progression in Chinese Children: A Crossover Trial

Start date: June 2014
Phase: Phase 4
Study type: Interventional

Orthokeratology is becoming popular for the treatment of myopia children. Many studies have shown that orthokeratology is effective in temporarily reducing refractive error, and is also helpful for controlling myopia progression. However, the mechanism for its slowing myopia progression and rebound effect after the treatment have not been clearly studied. In addition, the effect of orthokeratology among Chinese children has not been evaluated with randomized controlled trial.This study is to assess the effect of orthokeratology versus spectacles on myopia progression in school-aged Chinese children during two years.

NCT ID: NCT02180347 Completed - Myopia Clinical Trials

Contact Lenses and Myopia

CLAM
Start date: June 2014
Phase: N/A
Study type: Observational

The objective of this study is to determine if multifocal contact lenses affect accommodation and/or binocular vision when worn by pediatric patients. This will be accomplished through subjective and objective accommodative and binocular experiments in children wearing single vision and multifocal soft contact lenses.

NCT ID: NCT02175940 Completed - Clinical trials for Myopic Choroidal Neovascularization

VEGF and PEDF in Patients With Myopic Choroidal Neovascularization

Start date: July 2013
Phase: N/A
Study type: Observational

This was a prospective, case-control study investigating aqueous levels of VEGF and PEDF in eyes with mCNV treated with IVB.

NCT ID: NCT02175199 Completed - Myopia Clinical Trials

A Comparison of Two Color Contact Lenses in Habitual Clear Contact Lens Wearers

Start date: June 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the comfort of color contact lenses in a population of clear contact lens wearers who have an interest in wearing color contact lenses.

NCT ID: NCT02169635 Completed - High Myopia Clinical Trials

Macular Buckle With Three-armed Silicone

MBTAS
Start date: May 2013
Phase: N/A
Study type: Interventional

High myopia is characterized by prolonged axial length and posterior staphyloma, which result in choroid-retinal degeneration and vision decrease. At present, vitrectomy can lead to anatomical improvements, but an higher axial length and the presence of a sever posterior staphyloma remains to be the two most important risk factors for poor visual outcomes. For these reasons, a different surgical approach, including macular buckling, might be considered in those patients with extremely high degree of myopia, in order to counteract the traction exerted by the posterior staphyloma. Macular buckling with or without pars plana vitrectomy had been proved to be an effective way to resolve myopic staphyloma related foveoschisis, macular hole, and associated retinal detachment. In this study, we sought to investigate the safety and efficacy of a macular buckling technique using a three-armed silicone capsule to support the posterior staphyloma in high myopia.

NCT ID: NCT02161263 Completed - Myopia Clinical Trials

Quality of Vision and Quality of Life With LASIK

Start date: March 1, 2014
Phase:
Study type: Observational

The investigators are administering a validated questionnaire looking at patient reported quality of life and quality of vision after LASIK surgery

NCT ID: NCT02157909 Completed - Myopia Clinical Trials

DW Evaluation of Lotrafilcon B Lenses in a Modified Design

Start date: June 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate that Lotrafilcon B AIR OPTIX® AQUA sphere modified design lenses are noninferior to Lotrafilcon B AIR OPTIX® AQUA in overall lens fit by comparing the percent of subjects satisfying the "no re-fit" criteria in each treatment group.

NCT ID: NCT02150421 Completed - Myopia Clinical Trials

Impact of Electronic Devices on Myopia Development and Progression

Start date: September 2013
Phase: N/A
Study type: Observational

The aim of the stuy is to investigate the effects of the adoption of a curriculum with electronic devices for teaching materials and textbooks in Hong Kong schoolchildren on their changes in refractive error and visual function.