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Cataract clinical trials

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NCT ID: NCT06133660 Completed - Cataract Clinical Trials

Influence of Intravitreal Aqueous Tamponade on Lens Status and Ocular

Start date: October 30, 2020
Phase:
Study type: Observational

To observe the effects of vitreous cavity Balanced salt solution (BSS) tamponade on the state of the lens and related parameters of the eye, and whether the changes of the above parameters are correlated with age, gender, diabetes or not, etc., so as to provide references for the diagnosis and treatment of related diseases and scientific research.

NCT ID: NCT06118944 Completed - Cataract Clinical Trials

Outcomes of Bilateral Implantation of an Enhanced Monofocal Intraocular Lens

RCT_ICB00
Start date: November 11, 2019
Phase: N/A
Study type: Interventional

To evaluate and compare the visual outcomes of an enhanced monofocal intraocular lens (IOL) with two different monofocal IOLs in patients scheduled for bilateral cataract surgery.

NCT ID: NCT06075459 Completed - Cataract Clinical Trials

Post Marketing Clinical Evaluation Assessing the Visual Performance of Hanita Lenses "Intensity SL" Intraocular Lens

Post-op
Start date: March 1, 2023
Phase:
Study type: Observational [Patient Registry]

This clinical study will assess the safety and performance of Intensity SL IOL, 1 year post operation. The study will also evaluate the patient satisfaction of the implanted patients.

NCT ID: NCT06062771 Completed - Cataract Clinical Trials

Efficacy and Safety of the Use of Ophthalmic Viscosurgical Devices (OVD) FIDIAL PLUS vs IAL®-F During Cataract Surgery

Start date: July 23, 2022
Phase: N/A
Study type: Interventional

This is a Prospective, single-center, randomized, controlled, paired-eye, single-masked clinical investigation to compare the efficacy and safety of FIDIAL PLUS (bacterial derived 1.8% sodium hyaluronate OVD) and IAL®-F (comparable animal derived 1.8% sodium hyaluronate OVD) while used during phacoemulsification cataract surgery.

NCT ID: NCT05991960 Completed - Cataracts Clinical Trials

Evaluation of Real-World Data on the Performance of the TECNIS Odyssey™ IOL

Start date: September 11, 2023
Phase:
Study type: Observational

Retrospective collection of data from medical records, multicenter, post-market clinical follow-up study.

NCT ID: NCT05925894 Completed - Cataract Surgery Clinical Trials

Efficacy Mydrane ® for Cataract Surgery in Patients With Concomitant Primary Open Angle Glaucoma.

MIGA
Start date: March 18, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to compare Mydrane ®, mydriatic eye drops and Mydriasert ® in terms of pupil site stability, surgical time, visual field and anterior chamber configuration modifications among primary open angle glaucoma (POAG) patients during cataract extraction surgery.

NCT ID: NCT05915429 Completed - Cataract Clinical Trials

Predicting Lens Tilt Using Optical Coherence Tomography and Partial Least Squares Regression Modelling

Tilt
Start date: April 12, 2022
Phase:
Study type: Observational

Misalignment of IOLs can cause severe loss of visual quality. Different types of misalignment are known. Tilt is one type of misalignment that is thought to play a negative role for the optical performance in eyes with IOL designs, especially, if they have aspheric, toric or multifocal optics. Due to the fact that tilt has an influence on visual quality, the prediction of the post-operative tilt could improve IOL power calculaton significantly especially for toric IOLs. the Aim of this study is to measure tilt with two modern OCT based devices and one Scheimpflug camera and to predict the post-operative tilt using partial least squares regression.

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: NCT05868772 Completed - Cataract Clinical Trials

What is the Efficiency When Comparing Active Sentry at Low IOP vs Ozil at High IOP?

Start date: May 16, 2023
Phase:
Study type: Observational

The objective is to assess the efficiency of the Active Sentry handpiece at low intraocular pressure (IOP) compared with the Ozil at high IOP.

NCT ID: NCT05847114 Completed - Pain Clinical Trials

Evaluation of the Effectiveness of Stress Ball Practice During Cataract Surgery

Start date: October 26, 2022
Phase: N/A
Study type: Interventional

Cataract surgery is one of the most commonly performed and reliable surgeries among eye diseases. While cataract surgeries were performed under general or local anesthesia in previous years, they are now performed topically. Despite providing conscious sedation with agents such as benzodiazepines and opioids before and during surgery, patients experience pain, anxiety, and discomfort during the surgical procedure. One of the non-pharmacological methods used to relieve acute pain during surgical intervention is stress ball. It is also used to reduce pain and anxiety and increase patient comfort. The stress ball suppresses most of the nerves and muscles directly connected to the brain around the wrist and hand, stimulating nerve and muscle activity. This mechanism reduces the release of stress hormones, regulates blood pressure by providing relaxation and relief, and helps reduce anxiety and acute stress. When literature is examined, it is seen that stress ball application is effective on patients' pain, anxiety, and vital signs; however, no randomized controlled study has been found in which stress ball application was performed during cataract surgery. This study was planned to investigate the effect of stress ball application during cataract surgery on patients' anxiety, pain, and vital signs.