Clinical Trials Logo

Hyperopia clinical trials

View clinical trials related to Hyperopia.

Filter by:

NCT ID: NCT04632784 Recruiting - Myopia Clinical Trials

Clinical Trial With Artiflex Presbyopic

Start date: November 12, 2021
Phase: N/A
Study type: Interventional

The purpose of this clinical trial is to evaluate the effectiveness and safety of the multifocal Artiflex Presbyopic intraocular lens.

NCT ID: NCT04616144 Active, not recruiting - Hyperopia Clinical Trials

Fresh Corneal Lenticule Implantation in Hyperopic Patients With High Astigmatism

Start date: May 1, 2019
Phase: N/A
Study type: Interventional

The refractive combination of high hyperopia with high astigmatism is difficult to treat surgically. In addition, there are not many suitable options to offer such patients presenting with this condition. The method used at the EYE Hospital Pristina using fresh lenticule implantation by ReLex-SMILE is safe and effective method. Fresh Corneal Implantation is a safe treatment for hyperopia with high astigmatism comparing with refractive IOL implantation (loss of accommodation, endophthalmitis). Its primary objective is to increase visual acuity, accommodation process, patient satisfaction which makes patient to enjoy a happier life. We believe this study will be the future of refractive surgery for treating high hyperopia.

NCT ID: NCT04468022 Completed - Hyperopia Clinical Trials

Toric Trifocal IOL Treatment With High Astigmatism and Hyperopia vs SMILE Enhancement After Trifocal IOL Treatment

Start date: June 1, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to assess visual and refractive outcomes after Toric Trifocal lens implantation and visual outcomes after laser vision correction (LVC) - ReLex Smile to correct residual refraction after 6 months of Toric Trifocal (IOL) implantation.

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: NCT04297969 Completed - Clinical trials for Astigmatism Bilateral

Hyperopia Detection GCK With Glow Fixation

Start date: October 14, 2019
Phase:
Study type: Observational

"GoCheck Kids" has added to its iPhone 7+ smart phone with flash concentrator a non-accommodating glow box fixation target. In pediatric eye patients, the "GCK" with glow box is compared to cycloplegic refraction as well as School Bus Accommodation-relaxing skiascopy, "2WIN" photoscreener and "Retinomax."

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.

NCT ID: NCT04249505 Completed - Astigmatism Clinical Trials

Refractive Accuracy of "2WIN" and Portable Autorefractors

Start date: January 9, 2020
Phase:
Study type: Observational

Youth and some adults have photoscreening refractions and hand-held auto refraction before cycloplegia refraction during new and follow up eye examinations. Vector math is applied to each refraction to determine how closely the hand-held "dry" devices match actual refraction.

NCT ID: NCT04208750 Completed - Myopia Clinical Trials

Clinical Investigation of the Vision-R800 Device.

Start date: November 18, 2019
Phase: Phase 4
Study type: Interventional

Randomized, bilateral, cross-over dispensing study of a standard and VR800 refraction and associated spectacle lenses.

NCT ID: NCT04207749 Completed - Myopia Clinical Trials

Clinical Evaluation of a Daily Wear Silicone Hydrogel Lens

Start date: January 22, 2020
Phase: N/A
Study type: Interventional

The purpose of this clinical study is to assess 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 with frequent replacement.

NCT ID: NCT03881670 Completed - Myopia Clinical Trials

On-Eye Optical Quality of Lotrafilcon B Lenses Over 12 Hours

Start date: December 7, 2018
Phase: Phase 4
Study type: Interventional

The current study aims to systematically investigate the diurnal variation in the optical quality of soft contact lenses on eye throughout the day. Subject reported quality of vision will also be evaluated.