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Myopia clinical trials

View clinical trials related to Myopia.

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NCT ID: NCT03942419 Recruiting - Myopia Clinical Trials

Microdosed Atropine 0.1% and 0.01% Ophthalmic Solutions for Reduction of Pediatric Myopia Progression

Start date: June 3, 2019
Phase: Phase 3
Study type: Interventional

This study evaluates the progression of myopia in participants using microdosed atropine 0.01%, atropine 0.1%, or placebo ophthalmic solution. Eligible subjects will administer study medication daily in each eye for 48 months. Efficacy and safety assessments will be performed at visits scheduled for 1, 6, 12, 18, 24, 30 and 36 months after initiation of medication use. Subjects will be re-randomized at the 36 month visit, then followed at 6 month intervals for an additional year.

NCT ID: NCT03881358 Recruiting - Myopia Clinical Trials

Orthokeratology for High Myopia (OHM) Study

Start date: August 4, 2018
Phase: N/A
Study type: Interventional

This project aims to investigate/examine high myopic subjects on full correction ortho-k (using Topaz ortho-k lenses for high myopia) compared to subjects undergoing partial reduction ortho-k and their relationship with myopia and myopic progression.

NCT ID: NCT03865160 Recruiting - Myopia, Progressive Clinical Trials

Low-dose Atropine for Myopia Control in Children

AIM
Start date: October 19, 2021
Phase: Phase 2/Phase 3
Study type: Interventional

Myopia (nearsightedness) is the most common eye disorder. Only second to age, it is the main risk factor for major degenerative eye diseases such as glaucoma, macular degeneration or retinal detachment. Their risk increases with the degree of myopia. Hence, prevention of myopia and slowing its progression is of high relevance. Almost all clinical studies, including two large randomised clinical trials (RCT) were performed in Asia with Asian study participants. The results indicate that atropine eye drops can attenuate myopic progression in children, even in low concentrations thus minimizing unwanted side effects. However, the cumulative evidence is yet not strong enough to recommend their unrestricted use, especially in a Non-Asian population. We therefore intend to set up an adequately powered RCT comparing atropine 0.02% eye drops with placebo to validate previous findings and to test whether this therapeutic concept holds its promise in a European population.

NCT ID: NCT03552016 Recruiting - Refractive Errors Clinical Trials

Evaluation of Progression of Myopia in Children Treated With Vitamin B2 and Outdoor Sunlight Exposure

Start date: October 10, 2018
Phase: Phase 2
Study type: Interventional

The investigators plan on using riboflavin (a Vitamin that can easily be taken orally each day) and having the children involved in the study play outside (where there is UV light created by the sun) in order to prevent the eye from becoming progressively more near-sighted.

NCT ID: NCT03533647 Recruiting - High Myopia Clinical Trials

Development and Pathological Changes of High Myopia Among Children and Adolescents in China

Start date: May 14, 2018
Phase:
Study type: Observational

The study aims to observe the relationship between the changes of ocular structure parameters and pathological changes among children and adolescents with high myopia. Environmental factors and family history will also be collected to explore their impacts on high myopia progression.

NCT ID: NCT03516357 Recruiting - Myopia Clinical Trials

Effects on Ocular Parameters of Myopic Eyes After Orthokeratology in Myopic Children

Start date: January 11, 2018
Phase:
Study type: Observational

Effects on Ocular Parameters of Myopic Eyes After Orthokeratology in Myopic Children

NCT ID: NCT03446300 Recruiting - High Myopia Clinical Trials

Shanghai High Myopia Study for Adults

SHMSA
Start date: January 1, 2016
Phase: N/A
Study type: Observational

High myopia retinopathy has become the first cause of irreversible blindness and severe visual impairment in Chinese adults, in order to avoid the blind and visual impairment caused by high myopia retinopathy, it is very necessary to research the mechanism of early visual impairment to prevent and control damages. Our recent research found that the decreasing of macular retina vascular density and subfoveal choroidal thickness, the increasing of Beta Zone area in optic atrophy and the rising of glycosylated hemoglobin in high myopia patients were significantly related to visual impairment, which suggested that the source of visual impairment was the abnormal structure changes surrounding optic and fovea, but so far there is no related study. We will conduct a 5 years prospective cohort study in the population of 2420 high myopia and controls which have established in college student population, working population and aged more than 50 years old population, using the latest OCT-A and SS-OCT to measure macular retina vascular density, subfoveal choroidal thickness, Beta Zone area in optic atrophy, combined with the semiparametric mixed effects model, we will analysis the prediction index between fundus structure parameters, blood biochemical index and individual characteristics prediction to explore the public health management mode of early prevention and treatment during high myopia population.

NCT ID: NCT03402100 Recruiting - Myopia, Progressive Clinical Trials

Eye Drops Study for Myopia Control in Schoolchildren

Start date: October 20, 2014
Phase: N/A
Study type: Interventional

The myopia prevalence in schoolchildren is high in Taiwan. The myopia progression is fast in children and often associated high myopia in later life. This prospective and randomized study to investigate the effect of myopia control in myopic children with ultra low concentrations of atropine eye drops and/or low concentrations of anti-allergic and inflammatory eye drops.

NCT ID: NCT03383731 Recruiting - Retinal Detachment Clinical Trials

A Study of a New Surgical Treatment of Macular Hole Retinal Detachment in High Myopia

Start date: April 7, 2017
Phase: N/A
Study type: Interventional

This study evaluates the surgical outcomes of inverted internal limiting membrane insertion combined with air tamponade in the treatment of macular hole retinal detachment (MHRD) in high myopia, and also to compare the treatment efficacy and safety between different surgical approaches of MHRD

NCT ID: NCT03376412 Recruiting - Presbyopia Clinical Trials

A Study to Evaluate the Raindrop Near Vision Inlay Under Flap or Within Pocket

Start date: December 8, 2017
Phase: Phase 4
Study type: Interventional

The objective of this study is to evaluate the Raindrop® Near Vision Inlay for the improvement of near vision in presbyopes implanted under a corneal flap or within a small-incision pocket.