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Refractive Errors clinical trials

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NCT ID: NCT01484028 Completed - Clinical trials for Refractive Ametropia

Evaluation of the Performance of Two Contact Lenses Compared to a Marketed Lens

Start date: November 2011
Phase: N/A
Study type: Interventional

This study will serve to evaluate and compare the performance of two new lenses to a marketed lens.

NCT ID: NCT01461811 Completed - Myopia Clinical Trials

Prospective Study of an Investigational Toric Soft Contact Lens

Start date: December 2011
Phase: N/A
Study type: Interventional

The purpose of this study was to demonstrate substantial equivalence of an investigational toric soft contact lens to the commercially available Focus® DAILIES® Toric soft contact lens when worn in a daily wear, daily disposable mode for three months.

NCT ID: NCT01444313 Completed - Refractive Errors Clinical Trials

Prospective Study of the Health Benefits of Ultra-Violet Filtering Contact Lenses

Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the short-term protective effect of Ultra-Violet filtering contact lenses on macular pigment ocular density.

NCT ID: NCT01444053 Completed - Refractive Errors Clinical Trials

Retrospective Study of the Health Benefits of Ultra-Violet Filtering Contact Lenses

Start date: June 1, 2011
Phase: N/A
Study type: Observational

The purpose of this study is to examine the long term effect of ultra-violet filtering contact lenses on macular pigment density (MPOD) and accommodative function.

NCT ID: NCT01440322 Completed - Refractive Error Clinical Trials

AIR OPTIX® COLORS Registration Trial

Start date: September 2011
Phase: N/A
Study type: Interventional

The purpose of this study was to evaluate the subjective and objective performance and the physiological response to AIR OPTIX® COLORS soft contact lenses compared with AIR OPTIX® AQUA contact lenses in participants with normal eyes and prescription needs.

NCT ID: NCT01430247 Completed - Refractive Errors Clinical Trials

Vision Screening for the Detection of Amblyopia

Start date: September 12, 2011
Phase: N/A
Study type: Interventional

INTRODUCTION. Amblyopia is defined as the loss of visual acuity (VA) in one or both eyes, without any obvious structural or pathological anomalies. Amblyopic eye should be able to regain some VA if treatment is initiated before the age of seven. It is the leading cause of monocular blindness in the 20- to 70-year olds with prevalence 2-5%. Amblyopia is mainly monocular, hence children are general asymptomatic. VA testing is the only reliable method of detecting amblyopia, and the fourth year of life is considered best for vision screening programs. AIM: The purpose of the study is to reduce the preventable vision loss. The main goal of the study is to evidence the problem of amblyopia in Zagreb and to release a model for formal, government directed vision-screening program as a Croatian public health policy. HYPOTHESIS. In Croatia, the prevalence and actual effect of amblyopia and amblyogenic factors, along with treatment efficacy is impossible to quantify, since no population-based studies have been performed regarding this issue. In addition, national screening of preschool children does not exist, while the school-entry screening is prescribed by law. The object of the study is to determine the prevalence of amblyopia in a 4-4.5 year old children of The Town of Zagreb, the efficacy of screening and effectiveness of treatment on reducing amblyopia prevalence. The primary hypothesis is defined: screening of visual acuity monocularly at distance and near in 4-4.5 year old children in Zagreb is effective in detecting amblyopia. PATIENTS AND METHODS: Monocular vision of about 7000 children/ year aged 4-4.5 for whom both parents gave consent is to be tested with Lea chart at near (40cm) and distance (3m) in the kindergartens of The Town of Zagreb. The criterion for referral to complete ophthalmological examination is VA <0.8.

NCT ID: NCT01342393 Completed - Refractive Error Clinical Trials

Proof of Concept Study for First-Sight Refractive Error Correction: Direct Comparison to Manifest Refraction and Autorefraction Results

Start date: April 2011
Phase: N/A
Study type: Observational

Proof of concept study is to compare the best corrected visual acuity obtained via First-Sight lenses with the clinical "gold standard" of manifest refraction and autorefraction.

NCT ID: NCT01322919 Completed - Myopia Clinical Trials

Safety and Efficacy Study to Evaluate the Treatment of Both Near and Distance Vision in a Simultaneous Laser Procedure

Supracor
Start date: April 2010
Phase: Phase 3
Study type: Interventional

By using a new software two consecutive laser treatments have been combined to correct the distance vision and to provide a near vision component in addition to the first treatment. This study will help us to answer 2 questions: 1. How accurately this combined technique corrects distance and near vision 2. Whether the correction is adequate to remove the complete need for supplementary near spectacles

NCT ID: NCT01233089 Completed - Refractive Error Clinical Trials

Fitting Children With Contact Lenses

COPPER
Start date: September 2010
Phase: N/A
Study type: Interventional

The purpose of this three-month study is to compare the quality of life and ease of fit among children wearing investigational single-vision contact lenses, commercially marketed single-vision contact lenses, and commercially marketed multifocal contact lenses.

NCT ID: NCT01220466 Completed - Refractive Error Clinical Trials

Performance and Acceptability of iDesign

Start date: October 2010
Phase: N/A
Study type: Interventional

The results of this trial will demonstrate that the iDesign System performs as intended and is acceptable in a clinical setting.