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Refractive Errors clinical trials

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NCT ID: NCT05449015 Recruiting - Myopia Clinical Trials

Study on the Effect of Two Ways of Cycloplegia on Biological Parameters of Ciliary Muscle

Start date: December 22, 2020
Phase: Phase 4
Study type: Interventional

Atropine has a ciliary muscle-paralysing effect and causes hyperopic drift. Besides, atropine has been proven to slow the progression of myopia. Many studies have suggested that atropine can increase the thickness of the choroid. However, few studies have discussed changes in the ciliary muscle after treatment with atropine or other cycloplegic agents. This study aimed to assess the difference in ciliary muscle morphology before and after two different cycloplegic agents and to analyze the correlation between the changes of ciliary muscle biological parameters and the changes of eye axis, spherical equivalent, lens diopter, choroidal thickness, etc. One hundred and forty-four children would be randomly assigned 1:1 to the 1% atropine group and the tropicamide group. This study might provide clinical evidence for the role of regulatory factors in the occurrence and development of myopia.

NCT ID: NCT05447845 Recruiting - Cataract Clinical Trials

Rapid Computerized Visual Acuity Test

Start date: January 1, 2019
Phase:
Study type: Observational

A novel computerized visual acuity test was developed and tested on both healthy persons and patients with ocular conditions. Visual acuity outcomes of the computerized test will be compared to the Early Treatment Diabetic Retinopathy Study (ETDRS) in measures of reproducibility, accuracy and numbers of questions.

NCT ID: NCT05366543 Recruiting - Error, Refractive Clinical Trials

Errors of Refraction Among Primary School Children

Start date: January 3, 2022
Phase:
Study type: Observational

This study will include primary school children to evalute their refraction and follow those who will wear glasses to detect their compliance. Visual acuity will be measured using autorefractometer after cycloplegic eye drops 3 times and glasses will be prescribed for those who are needed. Follow up of the students to detect their compliance of wearing correction.

NCT ID: NCT05338411 Recruiting - Precocious Puberty Clinical Trials

Effect of Exogenous Growth Hormone on Ocular Findings

Start date: March 20, 2022
Phase:
Study type: Observational

Body size and eye function play an essential role in adapting to the environment and human survival. Growth hormone is commonly recognized by its effect on the height of individuals; Although from an evolutionary perspective, the effects of growth hormone on eye development are more important. Although the effect of growth hormone on eye development has not been accurately determined, the results of a number of studies suggest the effect of growth hormone on eye development. Despite the large number of studies that have investigated the effects of growth hormone on height growth, there are few studies that have investigated the effects of growth hormone on the eye. To the best of our knowledge, no study has been conducted to investigate the effect of growth hormone on ocular findings of patients with early or precocious puberty. Therefore, we intend to investigate the effect of growth hormone on ocular findings of patients with early or precocious puberty.

NCT ID: NCT05336799 Recruiting - Myopia Clinical Trials

Prevalence and Environmental Factors for Myopia Among Chinese School-aged Children and Adolescent in Tianjin

Start date: March 1, 2021
Phase:
Study type: Observational

The high prevalence of myopia has become a global public health problem. The study amied to investigate the prevalence and progression of myopia associated with social environmental factors in Tianjin, a Chinese megacity in north China.

NCT ID: NCT05325021 Recruiting - Refractive Errors Clinical Trials

Correction of Anisometropic Amblyopia in Children.

Start date: April 2, 2022
Phase:
Study type: Observational

Anisometropic amblyopia among children in school age may affects quality of life and educational progress of children.

NCT ID: NCT05250986 Recruiting - Refractive Errors Clinical Trials

Comparison of Visual Acuity Performed in Office Versus In Residence

VA IR vs IO
Start date: February 14, 2022
Phase:
Study type: Observational

GoCheck has developed and deployed a home-based visual acuity test that may be used in-office or in residence. The test methodology utilizes modified ATS and ETDRS protocols with Sloan optotypes, crowding bars and sophisticated algorithms. The objective of this study is to determine if the results of the GoCheck visual acuity test performed in an office setting correlate to the same testing when implemented in the residence

NCT ID: NCT05119543 Recruiting - Myopia Clinical Trials

Refractive Error in Chinese Students

Start date: January 1, 2018
Phase:
Study type: Observational

This cohort study aimed to assess the change of refractive status in Chinese school children.

NCT ID: NCT05059041 Recruiting - Down Syndrome Clinical Trials

Dilated Versus Non-Dilated Wavefront Corrections for Patients With Down Syndrome

Start date: May 6, 2022
Phase: Phase 2
Study type: Interventional

Individuals with Down syndrome (DS) live with visual deficits due, in part, to elevated levels of higher-order optical aberrations (HOA). HOAs are distortions/abnormalities in the structure of the refractive components of the eye (i.e. the cornea and the lens) that, if present, can result in poor quality focus on the retina, thus negatively impacting vision. HOAs in the general population are overall low, and thus not ordinarily considered during the eye examination and determination of refractive correction. However, for some populations, such as individuals with DS, HOAs are elevated, and thus the commonly used clinical techniques to determine refractive corrections may fall short. The most common clinical technique for refractive correction determination is subjective refraction whereby a clinician asks the patient to compare different lens options and select the lens that provides the best visual outcome. Given the cognitive demands of the standard subjective refraction technique, clinicians rely on objective clinical techniques to prescribe optical corrections for individuals with DS. This is problematic, because it may result in errors for eyes with elevated HOA given that these techniques do not include measurement of the HOAs. The proposed research evaluates the use of objective wavefront measurements that quantify the HOAs of the eye as a basis for refractive correction determination for patients with DS. The specific aim is to determine whether dilation of the eyes is needed prior to objective wavefront measurements. Dilation of the eyes increases the ability to measure the optical quality of the eye and paralyzes accommodation (the natural focusing mechanism of the eye), which could be beneficial in determining refractions. However, the use of dilation lengthens the process for determining prescriptions and may be less desirable for patients.

NCT ID: NCT05049070 Recruiting - Refractive Errors Clinical Trials

Study to Evaluate the Reliability, Validity and Safety of Subjective Mobile Refraction

Start date: September 15, 2021
Phase: N/A
Study type: Interventional

This study evaluates the reliability, validity and safety of a self administered, subjective refraction test via a mobile medical app (GoEyes) as compared to standard of care subjective manifest refraction performed by a health care provider, in subjects who have no known ocular disease or condition other than refractive error.