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Myopia clinical trials

View clinical trials related to Myopia.

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NCT ID: NCT02500368 Completed - Myopia Clinical Trials

A Dispensing Clinical Trial of a Study Test Silicone Hydrogel Lens Against Control Lens Over 1 Week

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

This is a 1-week dispensing, double-masked, randomized, bilateral study comparing the test lens against the control lens.

NCT ID: NCT02430428 Completed - Myopia Clinical Trials

Correction of Myopia Wtih or Without Astigmatism Using the VisuMax™ Femtosecond Laser

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

The objective of this clinical trial is to evaluate the safety and effectiveness of the Carl Zeiss Meditec VisuMax™ Femtosecond Laser lenticule removal procedure for the reduction or elimination of myopia from ≥ -1.00 D to ≤ -10.00 D with ≤ -3.00 D cylinder (myopia with or without astigmatism) and MRSE ≤ -11.50 D.

NCT ID: NCT02423109 Completed - Myopia Clinical Trials

Bilateral Dispensing Study of Fanfilcon A Toric Versus Enfilcon A Toric Lenses

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

Bilateral dispensing clinical trial of fanfilcon A toric lens verses enfilcon A toric lens over two weeks.

NCT ID: NCT02406495 Completed - Myopia Clinical Trials

Clinical Performance of Habitual Wearers of Bioclear 1-day Lenses When Refitted With Biomedics 1-day Extra for 1 Week

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

Open label, 1-week daily disposable, dispensing study

NCT ID: NCT02366923 Completed - Myopia Clinical Trials

Dehydration of Stenfilcon A Contact Lenses Versus Delefilcon A Contact Lenses

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

The study will explore in vivo lens dehydration rates across a 12hr wear period for the study lenses.

NCT ID: NCT02366910 Completed - Myopia Clinical Trials

Dehydration of Omafilcon A Contact Lenses Versus Delefilcon A Contact Lenses

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

The study will explore in vivo lens dehydration rates across a 12hr wear period for the study lenses.

NCT ID: NCT02354924 Completed - Myopia Clinical Trials

Clinical Evaluation of Two Daily Wear Silicon Hydrogel Contact Lens

Start date: June 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate that the VISCO (Olifilcon A) soft contact lens could be prescribed as a supportive care for myopic persons.

NCT ID: NCT02347631 Completed - Myopia Clinical Trials

DAILIES TOTAL1 Versus ACUVUE TruEye - Effects on the Biology of the Ocular Surface and Lid Margin

TruEyeTotal1
Start date: April 2016
Phase: N/A
Study type: Interventional

This is a prospective, single center, randomized, bilateral crossover, dispensing clinical trial to evaluate the effects of the water gradient lens, DAILIES TOTAL1, on the biology of corneal epithelium over two months of daily wear compared to wear of a control high oxygen permeable silicone hydrogel daily disposable contact lens, the ACUVUE TruEye; and to correlate these changes with alterations in the lid wiper, tear film and cellular changes at the limbus. The total proposed duration of this study is 12 months to ensure enrollment of up to 94 established contact lens wearers, with anticipated completion of 84. Data will be collected at baseline and following 2 months of daily wear for each lens type. Based upon data from the investigators previous contact lens clinical trials, a 1 month washout period is required prior to initiating lens wear and also between lens wear periods for the two types of lenses in order to eliminate any potential residual solution or lens effects on the corneal epithelium and restore homeostasis. The study is scheduled to commence upon Institutional Review Board approval.

NCT ID: NCT02346006 Completed - Myopia Clinical Trials

CHAMPS Eye Study - Myopia and Retinal Vascular Geometry in Relation to Physical Activity

Start date: February 1, 2015
Phase: N/A
Study type: Interventional

An increasingly physical inactive lifestyle in the Western World has led to a higher number of lifestyle -related diseases. The consequences are now already present in childhood with an increased prevalence of overweight, obesity, and diabetes. Inactivity is also accompanied by cardiovascular iseases and is also thought to be associated with an increased incidence of nearsightedness (myopia). Myopia is the most frequent eye disease globally, and causes severe personal and societal expenses and may additionally lead to secondary eye disorders such as retinal detachment, glaucoma, and cataract. The retina is the only place in the human body where it is possible to directly inspect the blood vessels (microvasculature). Photography of the eye background allows a noninvasive examination of the retinal structure in which it is possible to make measurements on the retinal blood vessels. It is well known that early vascular chances can be detected with this method and that there are correlation between these changes and systemic diseases, such as hypertension, stroke and other cardiovascular diseases. This study is a new subproject in The Childhood Health, Activity, and Motor Performance School (CHAMPS) Study Denmark, also known as the Svendborg Project. The project has a well-defined cohort with originally 1515 school students who since 2007 have been divided into two groups: schools with extra exercise during school hours and matched traditional schools. CHAMPS-DK aims to investigate the effect of increased physical activity on current and future health of children and adolescents. Thanks to this unique child cohort it is possible to investigate the correlation between physical activity, myopia and retinal vascular diameters in a large group of Danish schoolchildren. We want to study the degree and reversibility of physical activity and its effect on the development of myopia and retinal blood vessel changes. However, there is still a lack of knowledge about the correlation between physical activity and retinal vascular diameters in children. Furthermore, it is still unclear whether physical activity can prevent the development of myopia; such a realization could have far-reaching consequences in form of a modified approach to the necessity for exercise and, furthermore, potentially a significant socio-economic benefit.

NCT ID: NCT02345811 Completed - Myopia Clinical Trials

A Bilateral Dispensing Clinical Trial of Sapphire Lens Against Senofilcon A Lens Over 2 Weeks

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

To evaluate the clinical performance of an investigational silicone-hydrogel lens when worn on a daily wear modality over two weeks of lens wear.