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Capsule Opacification clinical trials

View clinical trials related to Capsule Opacification.

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NCT ID: NCT06379477 Not yet recruiting - Refractive Errors Clinical Trials

Correction of Refractive Error Surprises After Cataract Surgery in Adults

Start date: June 1, 2024
Phase: N/A
Study type: Interventional

A refractive surprise can be defined as the failure to achieve the intended postoperative refractive target or the presentation of unexpected and, unwanted post-operative refractive error. It can cause anisometropia or dominance switch and is a source of patient dissatisfaction due to unmet expectations.The best way to manage refractive surprise is to prevent it. The 2017 NICE guidelines on the management of cataracts provide advice on prevention of refractive surprise through accurate biometry, A-constant optimisation, intraocular lens (IOL) formula selection and avoiding wrong lens implant errors.Benchmark standards for NHS cataract surgery dictate that 85% of eyes should be within 1 dioptre (D) and 55% within 0.5D of target spherical equivalent refraction following surgery.

NCT ID: NCT06229756 Active, not recruiting - Cataract Clinical Trials

Clinical Results of Asqelio™ EDOF Toric Soft Hydrophobic Intraocular Lens After Cataract Surgery

Start date: October 26, 2022
Phase:
Study type: Observational

The goal of this observational study is to assess the clinical outcomes of binocular implantation of Asqelio EDOF Toric IOLs in healthy cataract patients. The main questions it aims to answer are: - What is the visual performance at different distances 3 months after implantation of Asqelio EDOF Toric in both eyes? - What is the amount of residual refractive error following the implantation? - What is the contrast sensitivity of patients 3 months after implantation of Asqelio EDOF Toric in both eyes? - What is the optical quality of the eye implanted with Asqelio EDOF Toric IOL? - What is the incidence and severity of visual symptoms after implantation of Asqelio EDOF Toric? - What is the level of patient satisfaction after implantation of Asqelio EDOF Toric? For this purpose, participants will be submitted to a comprehensive visual and refractive assessment, following common clinical practice, 3 months after binocular implantation of Asqelio EDOF Toric IOLs, and asked to complete visual symptoms and patient satisfaction questionnaires.

NCT ID: NCT06083025 Recruiting - Clinical trials for Posterior Capsule Opacification

Influence of CleaRing Open-capsule Device on Refractive Predictability in Cataract Patients (Part 2)

CleaRing
Start date: April 15, 2023
Phase: N/A
Study type: Interventional

The Hanita CleaRing device is an intraocular implant designed for inhibition of PCO leading to reduction in the Nd:YAG treatment rate. The device is implanted into the capsular bag after the extraction of the crystalline lens and prior to implantation of the IOL. The device is manufactured by Hanita Lenses from a hydrophilic acrylic co-polymer which is being used for the production of Intra-ocular lenses.

NCT ID: NCT06060041 Recruiting - Cataract Clinical Trials

IC-8 Apthera IOL New Enrollment Post Approval Study

Start date: September 8, 2023
Phase:
Study type: Observational

The purpose of this study is to verify the post-market safety of the IC-8 Apthera IOL after the treatment of posterior capsular opacification (PCO), an expected complication related to IC-8 Apthera IOL implantation.

NCT ID: NCT05988827 Recruiting - Cataract Clinical Trials

Effect of Minimizing Light Exposure Intensity on Macular Function After Cataract Surgery in Patients With Early or Intermediate AMD

EMERGING
Start date: September 14, 2023
Phase: N/A
Study type: Interventional

Cataract surgery is one of the most frequently performed surgical interventions worldwide. The microscope light-induced retinal toxicity after cataract surgery has been described in several reports even in short procedures; however, this potential toxicity has not been evaluated by objective criteria. Indeed, this retinal phototoxicity would be increased for patients with mild macular diseases such as early stages of AMD (Aged Macular Degeneration) (ie: drusen) which are frequently associated in elderly patients with cataract. The aim of the study will be to assess the potential functional macular effects by focal and multifocal ERG after cataract surgery with NGenuity by comparison to Standard Operating Microscope (SOM). This study would particularly address eyes at risk for macular toxicity like patients with early or intermediate AMD

NCT ID: NCT05912829 Recruiting - Aphakia Clinical Trials

Comparison of Two Different Intraocular Lenses Implanted With Yamane Technique

Start date: June 1, 2023
Phase:
Study type: Observational [Patient Registry]

In case of instability or rupture of capsular bag occurs during cataract surgery, Yamane technique is one of the options to fix intracocularlens' haptics. Yamane technique uses a double-needle technique that seamlessly fixes the haptics intrascleral by creating a scleral tunnel. Aberrations, IOL tilting or even dislocations might occur and influence the final outcome of IOL implantation. The aim of this study is the evaluation of the postoperative tilt of Kowa PU6AS using Yamane technique. Furthermore of the corrected and uncorrected visual acuity and the anterior chamber depth are being developed.

NCT ID: NCT05886283 Completed - Clinical trials for Effect of Cataract Surgery on Corneal Endothelium; About 2 Techniques

Qualitative and Quantitative Endothelium Changes After Cataract Surgery: Ultrasound Phacoemulsification vs Nanolaser Technique

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Purpose: The aim of this study was to evaluate corneal endothelial cell density and morphology, central corneal thickness, and best visual acuity using US phacoemulsification or Nanosecond laser technique. Setting: Department of ophthalmology, Nabeul, Tunisia. Design: Prospective cohort study. Methods: The study included eyes with nuclear cataract density grade 1, 2, 3, or 4 according to LOCS III, divided into two groups; Group 1 had conventional US, and group 2 had nanosecond laser. The Endothelial Cell Density (ECD), coefficient of variation (CoV) in cell size, percentage of hexagonal cells, central corneal thickness and best visual acuity were evaluated over 24 months.

NCT ID: NCT05834465 Not yet recruiting - Cataract Clinical Trials

High Intraocular Pressure After Cataract Surgery

Start date: July 1, 2023
Phase:
Study type: Observational

Effectiveness of anterior chamber drainage on the structure of the anterior chamber, the position of the intraocular lens and the shape of the corneal incision in the early stage of cataract surgery with high intraocular pressure

NCT ID: NCT05776095 Recruiting - Clinical trials for Lens Implantation, Intraocular

Evaluation of Safety and Performance Outcomes of Eyedeal IOL Implantation After Cataract Removal

Start date: November 10, 2023
Phase: N/A
Study type: Interventional

A cataract is the clouding of the natural lens in the eye and is very common as when getting older. A cloudy lens makes it difficult to see. A cataract is treated by removing the cloudy lens and replacing it with an intraocular lens (known as an IOL). The goal of this clinical trial is to determine if the Eyedeal® IOL can be safely implanted in a subject's eye and if it can replace efficiently the natural lens. Subjects will be asked to attend a total of seven visits for this study for a period of 12 months after surgery.

NCT ID: NCT05753787 Active, not recruiting - Cataract Clinical Trials

Eye Surface Properties After Using Dexamethasone Drops With and Without Preservatives in Patients After Cataract Surgery

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

The goal of this interventional, real world data study is to evaluate the impact of preservatives on the post-cataract ocular surface. The main question is to learn about an effect of preservatives on the eye surface. The study aims to answer some important questions: - if the usage of preservatives has an impact on the eye surface healing process after cataract surgery - if patient comfort and quality of life improve more or more rapidly with preservatives-free eye drops. Participants will be asked to undergo standard procedure of peri-cataract surgery care and in addition to survey about the ocular surface state. Researchers will compare group that takes preservatives-free dexamethasone 0.1% with standard dexamethasone 0.01% solution to see if post-surgery eye surface healing properties differ from both groups.