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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: NCT05305274 Completed - Myopia Clinical Trials

Age and Refraction in Predicting Myopia Progression in COVID-19

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

To determine the longitudinal changes of age and refraction in predicting myopia progression with risk under the coronavirus disease 2019 (COVID-19) pandemic in a 3-year follow-up of a Chinese cohort.

NCT ID: NCT05294328 Completed - Presbyopia Clinical Trials

Evaluation of the Safety and Effectiveness of Aceclidine/Brimonidine (LNZ101) and Aceclidine (LNZ100) in the Treatment of Presbyopia

Start date: May 5, 2022
Phase: Phase 2
Study type: Interventional

To evaluate the safety and effectiveness of Aceclidine/Brimonidine (LNZ101) compared with Aceclidine (LNZ100) and vehicle in the treatment of Presbyopia.

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: NCT05211739 Completed - Astigmatism Clinical Trials

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

Start date: February 15, 2022
Phase: N/A
Study type: Interventional

The purpose of this clinical study is to assess the clinical performance of an investigational toric soft contact lens compared to a commercially available toric contact lens in a crossover dispense trial when worn in a daily wear modality for 30 days, each study lens type.

NCT ID: NCT05209581 Completed - Refractive Errors Clinical Trials

Assessment of Visual Acuity in Refugee Population

Start date: January 24, 2022
Phase:
Study type: Observational [Patient Registry]

The present research process is a prospective clinical study that will be conducted under the auspices of the Democritus University of Thrace (DUTH) in the open accommodation structure for refugees and immigrants of Kavala, Kavala, Greece, and the Pre-Removal Detention Center (PROKEKA) for Foreigners of Kos, Kos, Greece. The study aims to assess the basic ophthalmological condition of the refugee/immigrant population and is developed in two main areas: 1. The recording of the ophthalmological care that the refugee/immigrant has received until his/her inclusion in the study through a structured questionnaire (eg previous examinations, spectacle utilization, pharmaceutical or other interventions, etc.) 2. The measurement of monocular best-spectacle corrected visual acuity in both eyes using a web-based visual acuity chart. Adult participants living in the two aforementioned centers will be recruited in a consecutive-if-eligible basis. All age groups will be proportionally represented (proportional age distribution).

NCT ID: NCT05166902 Completed - Ametropia Clinical Trials

Evaluation of Monthly Replacement Lenses in Habitual Soft Contact Lens Wearers Who Report Frequent Digital Devise Use

Start date: January 31, 2022
Phase: N/A
Study type: Interventional

To evaluate the clinical performance of two monthly silicone hydrogel contact lenses in habitual wearers of frequent replacement (FRP) lenses when worn for 1-month.

NCT ID: NCT05138783 Completed - Refractive Errors Clinical Trials

Clinical Performance of Two Daily Disposable Soft Contact Lenses

Start date: January 12, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the clinical performance of PRECISION1 contact lenses with Biotrue contact lenses.