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Lens Opacities clinical trials

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NCT ID: NCT04176965 Active, not recruiting - Cataract Clinical Trials

Investigation of the Safety and Effectiveness of a Trifocal IOL

Start date: May 30, 2022
Phase: N/A
Study type: Interventional

This study is a prospective, multicenter, randomized, double masked confirmatory trial comparing an investigational trifocal intraocular lens (IOL) and a commercially available monofocal IOL.

NCT ID: NCT04054427 Withdrawn - Cataract Clinical Trials

Implantation of a Trifocal Hydrophobic IOL in Patients That Underwent Refractive Surgery

Start date: November 2021
Phase: N/A
Study type: Interventional

Controlled, open label, prospective Post Market Clinical Follow-Up, single-center clinical study to investigate visual performance after implantation of a trifocal IOL (PhysIOL Pod L GF) in patients that underwent refractive surgery.

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: NCT03844828 Active, not recruiting - Cataract Clinical Trials

Clinical Study to Investigate Outcomes of Trifocal Toric IOL POD FT in Asian Eyes

Start date: March 25, 2019
Phase: N/A
Study type: Interventional

Prospective, controlled, single-surgeon, single-center clinical study to compare visual acuity outcomes to data obtained in a similar study by the same principal investigator on the trifocal IOL POD F (study no. PHY1802, ClinicalTrials.gov ID: NCT03688425)

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.

NCT ID: NCT03688425 Completed - Cataract Clinical Trials

Comparison of Clinical Outcomes POD L GF vs POD F GF in Asian Eyes

PHY1802
Start date: October 9, 2018
Phase: N/A
Study type: Interventional

Prospective, randomised, controlled, single-surgeon, single-center clinical study to compare the clinical outcomes of two trifocal IOLs differing in the dominance of additional power. The investigational device POD L GF shows dominance for the intermediate addition (+1.75 D), whereas the control device POD F GF shows dominance for the near addition (+3.5 D). Implantation of the IOLs is bilaterally.

NCT ID: NCT03423524 Completed - Cataract Clinical Trials

Clinical Study to Investigate Visual Performance of a Hydrophobic Monofocal IOL After Bilateral Implantation

PHY1801
Start date: May 2, 2018
Phase: N/A
Study type: Interventional

Prospective, non-randomised, open, controlled, single-center post-market clinical follow study about Micropure 1.2.3 IOL.

NCT ID: NCT03385070 Completed - Lens Opacities Clinical Trials

Salt Sensitivity Hypertension and Lens Opacities

Start date: March 15, 2017
Phase: N/A
Study type: Observational [Patient Registry]

Salt-sensitive hypertension (SSH) accounts for about the half of all Hypertension (HT) cases .In SSH, Na+/K+-ATPase activity is impaired. Impaired Na+/K+-ATPase activity in the lens epithelium results in cortical opacities in the peripheral equator of the lens. This study analyzed 305 patients with hypertension aged between 40 and 80 years and 124 non-HT controls. A total of 163 patients with HT who were admitted to the emergency service at least once with a minimum increase of 10% in their systolic and diastolic blood pressure after consuming salted food met the eligible criteria for HT and were included in the SSH group. A total of 142 patients who were previously diagnosed with HT but had no previous history were considered non-SSH. Two researchers examined the presence of cortical lens opacities biomicroscopically using the diffuse, direct, Scheimpflug, and retroillumination from fundus methods.

NCT ID: NCT03347981 Completed - Cataract Clinical Trials

Clinical Study to Compare Visual Performance of Two Trifocal IOLs

PHY1702
Start date: October 2, 2017
Phase: N/A
Study type: Interventional

Prospective, randomised, controlled, single-surgeon, single-center post-market clinical follow up study to compare the clinical outcomes of two trifocal IOLs with different material

NCT ID: NCT03306355 Completed - Cataract Clinical Trials

Comparison of Clinical Outcomes on Trifocal IOLs FineVision POD F GF and FineVision POD F in Asian Eyes

PHY1706
Start date: December 4, 2017
Phase: N/A
Study type: Interventional

Prospective, randomised, controlled, single-surgeon, single-center clinical study to compare the clinical outcomes of two trifocal IOLs with different material (hydrophobic and hydrophilic) from the same manufacturer. Implantation of the IOLs is bilaterally.