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Lens Opacities clinical trials

View clinical trials related to Lens Opacities.

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NCT ID: NCT05704686 Completed - Cataract Clinical Trials

Clinical Outcomes of an New EDOF IOL (Isopure®)

Start date: April 26, 2021
Phase:
Study type: Observational

Single-center, retrospective, open-label observational study aiming to evaluate visual outcomes and patient satisfaction after bilateral implantation of Isopure® EDOF-IOL with a mono-minovision target.

NCT ID: NCT05255029 Completed - Cataract Clinical Trials

Clinical Investigation of a Monofocal Toric Intra Ocular Lens (IOL) in Cataractous Eyes

PHY2107
Start date: December 24, 2021
Phase: N/A
Study type: Interventional

This is a Multi-center, single-arm and non-masked study whereby patients undergoing routine cataract surgery be implanted with a hydrophobic acrylic monofocal toric intraocular lens PODEYE TORIC (model POD T 49P).

NCT ID: NCT05235139 Completed - Cataract Clinical Trials

PMCF Study on Comparison of EDOF Lenses (Switzerland)

PHY2130
Start date: March 9, 2022
Phase: N/A
Study type: Interventional

Single center, prospective, randomised, controlled, double-blind post-market clinical follow-up (PMCF) study to compare the clinical outcomes of a premium monofocal intraocular lens (PhysIOL ISOPURE 1.2.3.) with clinical data obtained in a control group implanted with an EDOF IOL (Alcon Acrysof IQ Vivity).

NCT ID: NCT05055076 Completed - Cataract Clinical Trials

PMCF Retrospective Study Outcomes of a Monofocal Toric Intraocular Lens

Start date: August 1, 2021
Phase:
Study type: Observational

This is a monocentric retrospective, open-label clinical study in patients after unilateral or bilateral implantation of hydrophobic acrylic monofocal toric intraocular lens PODEYE TORIC and executed only with standard of care examinations. The investigational device is CE approved. The investigational device and all study products, including the devices used for the study examinations, have been used within the intended use specifications from the manufacturer. In addition, there were no invasive or other burdening examinations. The investigator is an accredited and experienced cataract surgeon and researcher. The primary endpoint is to determine rotational stability in a minimum of 120 eyes of patients with PODEYE TORIC IOL implantation after cataract surgery. Patients will be enrolled for the documentation and evaluation of retrospective data up to 6 months postoperatively.

NCT ID: NCT04933487 Completed - Cataract Clinical Trials

Rotational Stability Analysis of a Toric Monofocal IOL

PHY2013
Start date: August 26, 2014
Phase: N/A
Study type: Interventional

This is a single-center, prospective PMCF study whereby patients undergoing routine cataract surgery will have monolateral implantation of hydrophilic monofocal toric intraocular lens Ankoris.

NCT ID: NCT04875455 Completed - Cataract Clinical Trials

Premium Trifocal IOL Comparative Analysis

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

Short and long-term analysis of the refraction correction and optical image quality of modern premium intraocular lenses (IOLs) with the establishment of a database for quality assurance and optimization the computation constants of the lens power.

NCT ID: NCT04874376 Completed - Cataract Clinical Trials

PMCF Retrospective Study Outcomes of a Premium Monofocal IOL

PHY2110
Start date: May 24, 2021
Phase: N/A
Study type: Interventional

Multicentric, retro- / prospective, open-label, observational PMCF study to investigate visual performance, contrast sensitivity and patient satisfaction after mono- or bilateral implantation of Isopure 1.2.3. intraocular lenses following cataract surgery. The study treatment itself is not part of this observational clinical investigation. Only patients that already have been implanted with the device under investigation qualify for this retro- prospective observational clinical study.

NCT ID: NCT04699266 Completed - Cataract Clinical Trials

Clinical Investigation of the Multifocal IOL POD F GF in Cataracteous Eyes

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

To evaluate effectiveness and safety of the POD F GF Intraocular Lens (IOL) when implanted to replace the natural lens following cataract removal

NCT ID: NCT03974451 Completed - Cataract Clinical Trials

A Comparison of FineVision Intraocular Lenses vs Symfony Intraocular Lenses

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

This is a prospective randomised open-label study with the aim to compare the visual performance of the trifocal FineVision® IOL versus the extended range of vision Symfony® IOL after phaco-emulsification cataract surgery.

NCT ID: NCT03796624 Completed - Cataract Clinical Trials

Clinical Outcomes of MICROPURE and PodEye Monofocal Intraocular Lenses

PHY1803
Start date: February 12, 2019
Phase: N/A
Study type: Interventional

Prospective, non-randomised, open, controlled, single-center post-market clinical follow study about Micropure 1.2.3. and PODEYE intraocular lenses.