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Myopia clinical trials

View clinical trials related to Myopia.

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NCT ID: NCT02131402 Completed - Myopia Clinical Trials

Clinical Performance of Hydrogel vs. Silicone Hydrogel Contact Lenses

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

The aim of this non-dispensing fitting study is to evaluate the subjective comfort, lens handling, lens fitting characteristics and visual acuity of different hydrogel lens designs versus silicone hydrogel lenses

NCT ID: NCT02130167 Completed - Myopia Progression Clinical Trials

Low Concentration Atropine for Myopia Progression in School Children

Start date: August 2012
Phase: N/A
Study type: Interventional

Myopia is the leading cause of blindness in Taiwan. The younger children with myopia, the higher risk of high myopia in later life and complications such as retinal detachment and maculopathy will occur. We have reported the low concentration of atropine (0.05%) with the effect on retarding the myopia progression. Recently the 0.01% atropine was also reported effective and with less visual side effects such as mydriasis. The aim of this study is to compare the efficacy in controlling myopia progression and visual side effects of 2 low concentration of atropine(0.05% vs 0.01%) in children aged 6-12 years with myopia of at least -0.5 diopters (D) and astigmatism of -1.50 D or less.

NCT ID: NCT02103309 Completed - Myopia Clinical Trials

Comparative Evaluation of Contact Lens Centering of DAILIES® AquaComfort Plus® Versus 1-DAY ACUVUE® MOIST® in Japan

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

The purpose of this study is to evaluate lens centration and subjective impressions of DAILIES® AquaComfort Plus® (DACP) lenses compared to 1-DAY ACUVUE® MOIST® (1DAM) lenses in ball sports players.

NCT ID: NCT02100410 Completed - Myopia Clinical Trials

On-Eye Evaluation of Contact Lens Axis Location

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

The purpose of this study was to evaluate the axis location of toric contact lenses after 3 minutes of wear. During this 1-visit study, each participant wore 3 pairs of study lenses of various design iterations (2-87-1, 2-87-2, 2-87-3) for an exposure time of approximately 30 minutes each. Each pair consisted of lenses of the same design iteration, 1 lens with embossed mark [TEST1 (T1), TEST3 (T3), TEST5 (T5)], worn on the right eye, and 1 lens without embossed mark [TEST2 (T2), TEST4 (T4), and TEST6 (T6)] worn on the left eye.

NCT ID: NCT02097030 Completed - Myopia Clinical Trials

Clinical Evaluation of Daily Disposable Contact Lenses

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

The objective of the study is to compare the overall subjective preference of filcon II 3 daily disposable silicone hyrogel contact lenses compared to etafilcon A and nelfilcon A daily disposable conventional hydrogel contact lenses.

NCT ID: NCT02094677 Completed - Myopia Clinical Trials

Daily Disposable Comparison Study

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

The objective of the study is to compare the overall subjective preference between two Daily Disposable hydrogel lenses when refitted into a third hydrogel lens.

NCT ID: NCT02091934 Completed - Myopia Clinical Trials

Wavefront-guided PRK vs Wavefront-optimized PRK

Start date: April 1, 2009
Phase: N/A
Study type: Interventional

The purpose of the study is to compare the results of PRKK surgery when using wavefront-guided excimer laser treatment compared to wavefront optimized excimer laser treatment in patients with nearsightedness with and without astigmatism

NCT ID: NCT02082743 Completed - Myopia Clinical Trials

Vision Care Intervention for Lower Grade School Children in Taiwan

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

The purpose of this study is making use of school policy- recess outside classroom (ROC7-11) for increasing the time spent outdoor during recess and encouraging children spent time outdoor up to 11 hours in each week to investigate the vision change, myopia onset and progression in these schoolchildren.

NCT ID: NCT02066922 Completed - Myopia Clinical Trials

A Comparative Study of Two Daily Disposable Contact Lenses in Higher Myopia Subjects

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

The purpose of this study is to compare the change from baseline in central corneal curvature at one week, between 2 silicone hydrogel lenses, in higher myopic subjects.

NCT ID: NCT02064660 Completed - Myopia Clinical Trials

The Efficacy and Safety of Periocular Acupoint Stimulation on Myopia Progression in Children

Start date: December 2013
Phase: Phase 1
Study type: Interventional

Myopia is widely one of the three commonly detected refractive errors. Myopia is usually managed by correction through glasses or contact lenses. Other alternative available include surgery, drugs and acupuncture. There are various therapeutic approaches and different points can be used in acupuncture treatment for myopia, such as auricular acupuncture, acupressure body acupuncture. However, the mechanism of acupuncture therapy for myopia is largely unknown. Furthermore, little information exists regarding the effects and safety of acupuncture for degenerative myopia in children. The investigators aimed to assess the overall effectiveness, safety of periocular acupressure for children with myopia The hypotheses of this study are as follows: Periocular acupressure is effective for myopia progression delay. The study aims to include 56 participants.