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Myopia clinical trials

View clinical trials related to Myopia.

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NCT ID: NCT03496701 Completed - Myopia Clinical Trials

Performance of Wearers of Stenfilcon A Contact Lenses After A Refit With Test Lenses

Start date: April 18, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to determine if habitual or adapted wearers of stenfilcon A control contact lenses can be refit into test lenses and be successful after one week of daily wear.

NCT ID: NCT03479827 Completed - Nearsightedness Clinical Trials

Measuring the Peripheral Optical Quality of The Eye

Start date: August 31, 2018
Phase:
Study type: Observational

The goal of the study is to quantify wavefront aberration profiles of the eye with and without contact lens across the visual field. This will enable us to investigate the impact of the aberration on retinal image quality.

NCT ID: NCT03471832 Completed - Myopia Clinical Trials

Clinical Evaluation of Stenfilcon A Contact Lenses

Start date: March 3, 2018
Phase: N/A
Study type: Interventional

This study is to evaluate the fitting performance of stenfilcon A contact lens (test) compared to narafilcon A contact lens (control).

NCT ID: NCT03465748 Completed - Myopia Clinical Trials

Effectiveness of Orthokeratology in Myopia Control

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

The high prevalence of myopia - especially in Asian countries - is well documented, as are the sight-threatening complications of high or degenerative myopia. Retinal detachment, glaucoma, vitreal degeneration and focal retinal changes may occur secondary to the progressive axial elongation of the eye with age. Specialty rigid lenses have long been shown to lessen this progression in the pediatric population; orthokeratology (ortho-k) lenses are worn at night and change the corneal topography to correct low to moderate amounts of myopia. Most of the studies on orthokeratology were conducted on Asian children. To the best of the investigators knowledge, no study has been done on African American (AA) children. The investigators' project seeks to investigate the efficacy of ortho-k in slowing axial elongation and myopic progression in AA children compared to that in other races.

NCT ID: NCT03456245 Completed - Myopia Clinical Trials

Comparing Low-cost Handheld Autorefractors - a Practical Approach to Measuring Refraction in Low Resource Settings

Start date: August 15, 2016
Phase:
Study type: Observational

Study compares four portable vision measurement and eye-imaging technologies in terms of accuracy and time and ease of use with older adult (ages 40-100) participants in a developing-country setting (India). Specifically, the five portable devices will be measured against the baseline of the traditional eye-examination techniques, including the use of eye charts and phoropters.

NCT ID: NCT03451877 Completed - High Myopia Clinical Trials

TGFB1 And LAMA1 Gene Polymorphisms in High Myopia

Start date: December 1, 2012
Phase: N/A
Study type: Interventional

The investigators aimed to investigate TGFB1 and LAMA1 gene polymorphisms in children with high myopia in order to determine the genetic basis of large myopic shifts causing severe visual impairment and complications. Seventy-four children with high myopia (≥6 diopters [D]; study group) and 77 emmetropic children (±0.5D; control group) were included. Genetic and polymorphism analyses were performed in the Medical Genetics Laboratory using DNA purified from the patients' blood samples.

NCT ID: NCT03433547 Completed - Macular Holes Clinical Trials

Effects of Macular Buckle Versus Vitrectomy on Macular Hole and Macular Detachment in Highly Myopic Eyes

Start date: January 30, 2018
Phase: N/A
Study type: Interventional

Full-thickness macular Hole associated with macular detachment is a one of the maculopathies of high myopia. There is controversy in the primary treatment for this situation. This study will compare the effects of macular buckling versus vitrectomy in a cohort of highly myopic eyes with this situation.

NCT ID: NCT03413085 Completed - Myopia Clinical Trials

To Evaluate the Efficacy and Safety of Multifocal Soft Contact Lens in Myopia Control

Start date: May 2, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to investigate the efficacy and safety of soft lens in myopia control.

NCT ID: NCT03408444 Completed - Visual Acuity Clinical Trials

Evaluating Soft Contact Lens Prototypes for Myopia Control

Start date: December 27, 2017
Phase:
Study type: Interventional

This is a multi-site, prospective, randomized, controlled, double-masked, four-arm-parallel-group, dispensing study. Each subject will be bilaterally fitted with one of four types of test articles and wear contact lenses of the assigned lens type during the entire course of the study. Test articles will be worn a minimum 8 hours per day and 5 days per week (subjects will be encouraged to wear study contact lenses 10 hours or more per day and 7 days per week) in a daily disposable modality for a minimum of 6 months and up to 1 year for a total of 7 scheduled visits.

NCT ID: NCT03384628 Completed - Myopia Clinical Trials

An Evaluation Of The Fitting Success Rate Of Senofilcon A Soft Contact Lenses In Three Designs.

Start date: January 26, 2018
Phase: N/A
Study type: Interventional

This study will compare the on-eye fitting characteristics of three types of contact lenses. Each lens pair will be worn for 30 to 45 minutes before assessment and the results will be compared to mathematically calculated fitting characteristics.