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Cataract clinical trials

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NCT ID: NCT05504343 Completed - Cataract Clinical Trials

Assessing The Visual Performance Of Hanita Lenses "Intensity SL" Intraocular Lens

Start date: December 27, 2021
Phase: N/A
Study type: Interventional

The Hanita Lenses Intensity SL IOL is intended for implantation in the capsular bag in the posterior chamber in order to replace the crystalline lens of the eye to attain visual correction of aphakia in adult patients in whom a cataractous lens has been removed, who desire improved uncorrected vision, useful near, intermediate and far visual functions, and reduced spectacle dependence.

NCT ID: NCT05495555 Completed - Cataract Clinical Trials

The Cutting Efficiency of Hybrid Tips in Different Grades of Cataract

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

The objective is to assess the efficiency (as measured by phaco time, aspiration time, and fluid use) of the hybrid tip in removing cataract grade 3 & 4 in high and low intraocular pressure (IOP) settings.

NCT ID: NCT05494177 Completed - Cataract Clinical Trials

Comparison of Premium Monovision and Bilateral Implantation of Trifocal Diffractive Intraocular Lenses

Start date: August 1, 2022
Phase:
Study type: Observational [Patient Registry]

Primary objective of this study is to compare two presbyopia correction surgical techniques, specificaly premium monovision, in which the dominant eye is corrected with an extended depth of field intraocular lens and the non-dominant eye with a trifocal diffractive intraocular lens, and the bilateral implantation of trifocal diffractive intraocular lenses.

NCT ID: NCT05491798 Recruiting - Cataract Clinical Trials

A Big Data-based Cohort Study for Cataract Patients

Start date: July 1, 2020
Phase:
Study type: Observational [Patient Registry]

Cataract is an important cause of blindness and visual impairment worldwide. At present, the only effective treatment method is surgery. The visual function of most patients can be significantly improved after surgery, but there are still 5-20% of patients whose visual function cannot be improved after surgery. Previous studies have found that the surgical complications and postoperative visual function of cataract patients are closely related to the condition of the fundus, but the current fundus camera cannot perform clear fundus imaging of cataract patients, and the existing potential visual inspections, such as retinal visual inspection, are also inaccurate. Predict postoperative visual acuity. Therefore, there is an urgent need for a reliable postoperative effect prediction system for cataract patients to provide reference for both ophthalmologists and patients. This study intends to collect patient medical record information and traditional/ultra-wide fundus photos and other multi-modal data. Firstly, this study will use artificial intelligence technology to enhance fundus photos of cataract patients to obtain clearer fundus photos. Then this study will use both medical record information and traditional/ultra-wide fundus photographs to predict postoperative vision and visual function of cataract patients.

NCT ID: NCT05489198 Not yet recruiting - Cataract Clinical Trials

Cataract Surgery Technique and Ocular Clarity

Start date: September 2022
Phase: N/A
Study type: Interventional

The goal of this study is to study the restoration of quality of vision, expressed as straylight, in the immediate period after cataract surgery with two different phacoemulsification technologies.

NCT ID: NCT05488769 Terminated - Cataract Clinical Trials

Visual Outcomes and Patient Satisfaction After Bilateral Implantation of Non-diffractive EDOF IOL Made of a New Hydrophobic Acrylic Material

Start date: August 25, 2022
Phase:
Study type: Observational

The objective is to measure the range of vision and patient reported visual disturbances after bilateral implantation for this unique non-diffractive extended depth of focus (EDOF) intraocular lens (IOL) made from the Clareon material.

NCT ID: NCT05481125 Completed - Cataract Clinical Trials

Clareon Toric vs Eyhance Toric

Start date: October 10, 2022
Phase: N/A
Study type: Interventional

The primary purpose of this study is to compare the Clareon/Clareon Toric Intraocular Lenses (IOLs) to the Eyhance/Eyhance Toric IOLs in binocular Best Corrected Distance Visual Acuity (BCDVA) at 3 months postoperative.

NCT ID: NCT05480839 Recruiting - Clinical trials for Early Anesthesia vs Standard Anesthesia

Manual Immediately Sequential Bilateral Cataract Surgery (M-ISBCS) vs Refractive Laser-Assisted Immediately Sequential Bilateral Cataract Surgery (ReLA-ISBCS)

Start date: June 1, 2022
Phase: N/A
Study type: Interventional

The focus of this study is to assess the differences in patient perceptions of pain undergoing cataract surgery by using the Refractive Laser-Assisted Cataract Surgery (ReLACS) technique compared to the standard Manual Cataract Surgery (MCS) technique using an immediately sequential bilateral approach. This study also aims to further explore difference in patients' perceptions of pain depending on timing of neurolept anesthesia in the ReLACS technique. The importance of this study is appreciated patient perception of pain during ReLACS, which is an emerging technique for cataract surgery and has been sparsely reported on to date. This investigation will include the analysis of various surgical, ocular, medical, and psychosocial metrics of patients undergoing both ReLACS and MCS at Uptown Eye specialist.

NCT ID: NCT05472844 Recruiting - Pediatric Cataract Clinical Trials

The Cohort Study of Pediatric Cataract

Start date: August 22, 2022
Phase:
Study type: Observational

This retrospective-prospective bidirectional cohort study aims to observe ocular parameter changes, different surgical/vision recovery strategies and postoperative adverse effects among young children with cataract. The influence on psychology and cognitive function will be taken into consideration as well.

NCT ID: NCT05465447 Not yet recruiting - Cataract Clinical Trials

The Long-term Outcome After Toric Intraocular Lens Implantation

Start date: July 2022
Phase:
Study type: Observational

Corneal astigmatism is refractive error that impairs uncorrected visual acuity. When patients undergo cataract surgery, implantation of toric IOL is deemed the most effective choice for correcting corneal astigmatism and reducing postoperative spectacle dependence. Previous studies report that the visual effects and rotational stability of toric IOLs are well maintained over 1- or 2-year follow-up periods. However, the long-term changes in the effects of toric IOLs remain unclear.