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Refractive Errors clinical trials

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NCT ID: NCT04437732 Completed - Presbyopia Clinical Trials

Apioc Presbyopic Contact Lens

Start date: November 11, 2019
Phase: N/A
Study type: Interventional

In this study, you will wear an invesetigational contact lens, Apioc-P or Apioc-PT, the way you wear your current contact lenses for approximately one month (no more than 35 days).

NCT ID: NCT04429659 Completed - Refractive Errors Clinical Trials

Changes in Refractive Error in Patients With Both Partially Refractive Esotropia and Amblyopia

Start date: January 2, 2019
Phase:
Study type: Observational

To investigate changes in refractive errors and evaluate clinical outcomes of strabismus surgery in patients with both amblyopia and partially refractive esotropia (PAET).Amblyopic patients with PAET were enrolled. Non-amblyopic patients with full refractive accommodative esotropia (RAET) were included in the study as a control group. Preoperative and postoperative best corrected visual acuity (BCVA), spherical equivalent (SE), astigmatism, stereoacuity and deviations at near and distance were evaluated and statistically compared in the patient group. The mean BCVA, SE, astigmatism were compared between the patient and the control groups.

NCT ID: NCT04422990 Completed - Refractive Errors Clinical Trials

Clinical Evaluation of a Silicone Hydrogel Daily Wear Monthly Replacement Contact Lens

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

The purpose of this clinical study is to evaluate the safety and performance of an investigational soft contact lens compared to a commercially available soft contact lens when worn in a daily wear modality.

NCT ID: NCT04403542 Completed - Myopia Clinical Trials

Pilot Clinical Performance of a Silicone Hydrogel Lens for Up to Six Nights of Extended Wear

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

The purpose of this clinical study is to evaluate the on-eye performance of an investigational soft contact lens compared to a commercially available soft contact lens when worn continuously for up to 1 week.

NCT ID: NCT04352868 Withdrawn - Myopia Clinical Trials

Customizing Myopia Control With Multifocal Toric Contact Lens

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

This study will evaluate the ability of toric multifocal contact lens to reduce the change of myopia progression in children (aged 8-12) with myopic astigmatism.

NCT ID: NCT04346251 Recruiting - Refractive Errors Clinical Trials

Correlation Between Refraction and Biometric Parameters

Start date: November 1, 2017
Phase:
Study type: Observational

To document the refractive status of Chinese schoolchildren and evaluate the association between the degree of refraction and biometric parameters.

NCT ID: NCT04338880 Recruiting - Refractive Errors Clinical Trials

Academic Performance and Refractive Error

Start date: September 1, 2016
Phase:
Study type: Observational

Refractive errors constitute the leading cause of visual disability worldwide and that myopia progresses dramatically when students reach school age. Studies from different countries have reported inconsistent associations between educational outcomes and refractive errors. Therefore, our study aimed to assess the associations of high academic performance with ametropia prevalence and myopia progression in Chinese schoolchildren base on a multicohort observational design.

NCT ID: NCT04328207 Active, not recruiting - Cataract Clinical Trials

Providing Financial Incentives to Improve Adherence to Referral Eye Care Visits

Start date: November 18, 2020
Phase: N/A
Study type: Interventional

Glaucoma is a blinding eye disease increasingly common in older adults, particularly in African Americans, and often diagnosed late in the disease course. It is essential to develop novel health care models, utilizing telemedicine, to improve the ability to detect glaucoma at an earlier stage, and to provide a platform to manage this disease in community-based clinics so that further vision loss is prevented. Our goal is to improve the quality and accessibility of glaucoma detection and management among a vulnerable and at-risk segment of our population.

NCT ID: NCT04295499 Completed - Refractive Errors Clinical Trials

Safety and Effectiveness of the Qualis Contact Lens

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

Three-month, open-label, bilateral, parallel group, randomized, daily wear contact lens dispensing study.

NCT ID: NCT04283331 Recruiting - Myopia Clinical Trials

Anesthetic Impregnated Bandage Soft Contact Lens (BSCL) in Pain Management After Photorefractive Keratectomy (PRK)

Start date: June 1, 2020
Phase: Phase 4
Study type: Interventional

Compared to laser-assisted in situ keratomileusis (LASIK), Photorefractive Keratectomy (PRK) is associated with more discomfort and requires more downtime. However, it is oftentimes considered the preferred method of refractive surgery for patients with dry eye syndrome, high refractive errors, thin corneas, or those with more active lifestyles who may be more prone to dislodging their LASIK flaps. We hypothesize that the use of bandage contact lenses soaked in proparacaine will decrease pain levels compared to solely the use of bandage contact lenses after PRK.