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Lens Opacities clinical trials

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NCT ID: NCT06294405 Recruiting - Lens Opacities Clinical Trials

Intraocular Lens Implant Registry Study

Start date: February 21, 2024
Phase:
Study type: Observational [Patient Registry]

The goal of this registry study is to optimize the results with intraocular lens implants used in cataract surgery.

NCT ID: NCT06105190 Recruiting - Cataract Clinical Trials

Clinical Study to Evaluate Clinical Outcomes of LuxSmart IOL as Compared With LuxGood IOL

Start date: June 21, 2023
Phase: N/A
Study type: Interventional

This study is a multicentric, prospective, randomised, controlled, post-market clinical follow up (PMCF) study to investigate safety, visual outcomes and contrast sensitivity after bilateral implantation of either LuxSmart IOLs (study group) or LuxGood IOLs (control group).

NCT ID: NCT05875922 Recruiting - Cataract Clinical Trials

Comparison of ISOPURE and EYHANCE (Switzerland)

PHY2301
Start date: August 31, 2023
Phase: N/A
Study type: Interventional

This is a prospective randomised open-label study with the aim to compare the visual performance of the premium monofocal Isopure IOL versus the extended depth of focus Eyhance® IOL after phaco-emulsification cataract surgery.

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: NCT05588921 Recruiting - Lens Opacities Clinical Trials

LensAge to Reveal Biological Age

Start date: January 1, 2020
Phase:
Study type: Observational

Assessment of aging is central to health management. Compared to chronological age, biological age can better reflect the aging process and health status; however, an effective indicator of biological age in clinical practice is lacking. Human lens accumulates biological changes during aging and is amenable to a rapid and objective assessment. Therefore, the investigators will develop LensAge as an innovative indicator to reveal biological age based on deep learning using lens photographs.

NCT ID: NCT05458661 Not yet recruiting - Cataract Clinical Trials

Feasibility Investigation of Biometry and Tomography Measurements in a Heterogeneous Patient Cohort

BioBase
Start date: August 2022
Phase: N/A
Study type: Interventional

The planned clinical investigation will be conducted to acquire raw data for the development of the algorithm. The data acquisition is intended to obtain first impressions of the potential performance of the changed hardware and software components and to confirm the safety profile assessed by risk analysis.

NCT ID: NCT05290896 Recruiting - Cataract Clinical Trials

Correlations Between Lens Star and Phacoemulsification.

Start date: February 20, 2022
Phase: N/A
Study type: Interventional

To assess correlations between lens star biometry parameters and phacoemulsification in clinical practice.

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.