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Myopia clinical trials

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NCT ID: NCT04604405 Completed - Myopia Clinical Trials

Effects of 650nm Low Energy Light on Human Retina and Choroid Microcirculation

Start date: September 8, 2020
Phase: N/A
Study type: Interventional

This project is a single-center, prospective, self-controlled clinical study. It intends to select patients with simple medium and low degree myopia as subjects, and apply 650nm low-energy red light irradiation to the retina to observe its effect on macular microcirculation.

NCT ID: NCT04589091 Completed - Myopia Clinical Trials

Corneal Topography Asymmetry Indices Changes After Corneal Refractive Surgery

Start date: April 13, 2021
Phase:
Study type: Observational

To evaluate the changes that occur in the corneal indices after corneal refractive surgery either PRK or LASIK.

NCT ID: NCT04585646 Completed - Myopia Clinical Trials

A Two-Week Crossover Dispensing Evaluation Of Orion Daily Wear Soft Contact Lens

Start date: September 14, 2020
Phase: N/A
Study type: Interventional

The primary objective of the study is to evaluate the clinical performance of test lens (Orion) in comparison with control lens (Gemini) over a period of two weeks of wear.

NCT ID: NCT04536571 Completed - Myopia Clinical Trials

Vision Stability and Preference for Soft Toric vs. Soft Spherical Contact Lenses

Start date: September 3, 2020
Phase: N/A
Study type: Interventional

The principal hypothesis is to be tested in this work is that vision stability (the primary outcome measure) with a spherical contact lens correction vs. a toric contact lens correction will be the same.

NCT ID: NCT04528017 Completed - Myopia Clinical Trials

Clinical Comparison of 2 Daily Disposable Contact Lenses - Pilot Study 2

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the overall performance of PRECISION1 contact lenses when compared to Clariti 1-Day contact lenses.

NCT ID: NCT04527978 Completed - Myopia Clinical Trials

Clinical Comparison of 2 Daily Disposable Contact Lenses - Pilot Study 1

Start date: September 15, 2020
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the overall performance of PRECISION1 contact lenses when compared to Biotrue ONEday contact lenses.

NCT ID: NCT04524910 Completed - Clinical trials for Myopic Choroidal Neovascularization

A Study to Learn More About How Drug Aflibercept Works in Canadian Patients With Reduced Vision Caused by New Blood Vessels Growing in the Eye (Myopic Choroidal Neovascularization or mCNV)

REALM
Start date: June 16, 2021
Phase:
Study type: Observational

Being short sighted means that vision is blurry when looking at things far away. People with a condition called "pathologic myopia" are short sighted due to problems in the back layer of their eyes, also known as the retina. Some people with pathologic myopia can develop a serious condition called myopic choroidal neovascularization (mCNV). In people with mCNV, new blood vessels grow into the retina. These blood vessels can break, leaking blood or fluid into the retina. This can cause blurry vision or a loss of vision. In this study, researchers will find out more about how well drug aflibercept works and how safe it is in Canadian patients with mCNV. The researchers in this study will review information from the patients' eye doctor visits. The patients in this study will include Canadian men and women who started receiving aflibercept between May 2017 and August 2019. These patients were at least 18 years old and had not received treatment for their mCNV before. The researchers will look at the results of vision tests to find out how well the patients could read from a distance after they received aflibercept for 6 months. They will compare the results of these tests to before the patients received treatment. They will also learn more about how safe it is to have aflibercept injection into the eye.

NCT ID: NCT04492397 Completed - Myopia Clinical Trials

Comparing The Performance Of Two Different Daily Disposable Lenses (MIKI)

Start date: September 30, 2020
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate and compare the performance of study test lens to study control lens, when worn on a daily disposable modality over a period of approximately one week each

NCT ID: NCT04488887 Not yet recruiting - Healthy Clinical Trials

OCTA Metrics Repeatability and Reproducibility in Different Disorders

Start date: August 1, 2020
Phase:
Study type: Observational

Retinal imaging is a corner stone in diagnosis of most retinal disorders. Standard imaging techniques e.g. fluorescein angiography and color fundus photography have a lot of limitations including limited resolution, invasive nature in cases of fluorescein angiography, and inability to segment the retina, accordingly, and only 2D image is provided. Optical coherence tomography angiography (OCTA) is a recent noninvasive imaging technique that allows for volumetric visualization of eye vasculature. OCTA has shown promise in better elucidating the pathophysiology of several retinal vascular diseases. Swept-source OCTA uses long wavelength ̰ 1,050nm, which can penetrate through deeper layers of the eye and can traverse opacities of media such as cataracts, hemorrhages and vitreous opacities. Optical coherence tomographic angiograms can further be manually or automatically segmented with preprogrammed software to highlight individual layers of the retina, optic nerve head choriocapillaris, and choroid. The user can either analyze en face images extending from the inner limiting membrane to choroid or use automated views to locate a vascular or structural lesion within the retina. Different quantitative metrics has been extracted from enface OCTA images including vessel density, FAZ area, choriocapillaries flow deficit, intercapillary area and fractal dimension. These metrics are helpful in evaluation the retinal perfusion and used by physicians to assess various retinal vascular disorders. Although some previous literatures had discussed the repeatability of OCTA metrics, however, comprehensive evaluation of widely used metrics in various retinal condition has not be done. Additionally, recent data suggest that various methods of calculation of these metrics my yield final different results of the same metric.

NCT ID: NCT04476784 Completed - Myopia Clinical Trials

Clinical Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens

Start date: August 17, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the clinical performance of an investigational contact lens over 30 days of daily wear.