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Aphakia clinical trials

View clinical trials related to Aphakia.

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NCT ID: NCT03316885 Completed - Cataract Clinical Trials

Post-Market Clinical Investigation of the Clareon® IOL

Start date: March 14, 2018
Phase: N/A
Study type: Interventional

The primary purpose of this study is to evaluate the long-term (3 years) visual acuity and adverse event outcomes for the Clareon® Intraocular Lens (IOL). A comparison to historical safety and performance endpoint (SPE) rates as reported in the European Standard International Organization for Standardization (EN ISO) 11979-7:2014 will be conducted at one year. The secondary purpose of this study is to evaluate the visual acuity outcomes with the Clareon IOL at Years 2 and 3.

NCT ID: NCT03054649 Completed - Cataract Clinical Trials

ClarVista HARMONI Toric Trial With Intraoperative Exchange

Start date: June 28, 2016
Phase: N/A
Study type: Interventional

The purpose of this study was to demonstrate the safety and effectiveness of the HARMONI® Modular Intraocular Lens System with a toric optic in subjects with pre-existing corneal astigmatism in need of cataract surgery.

NCT ID: NCT03050697 Completed - Cataract Clinical Trials

Evaluation of the Safety and Performance of the HARMONI® Toric Lens

Start date: September 28, 2016
Phase: N/A
Study type: Interventional

The purpose of this study was to evaluate the safety and effectiveness of the HARMONI® Modular Intraocular Lens System with a toric optic (HMTIOL) in subjects with pre-existing corneal astigmatism in need of cataract surgery.

NCT ID: NCT02418871 Completed - Aphakia Clinical Trials

Evaluation of the FluidVision Accommodating Intraocular Lens (AIOL) With an Improved Injector System

Start date: March 13, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the clinical outcomes of an investigational IOL in patients undergoing cataract extraction and intraocular lens implantation using an improved injector system.

NCT ID: NCT02049567 Completed - Aphakia Clinical Trials

Clinical Evaluation of the FluidVision Accommodating Intraocular Lens (AIOL)

Start date: January 14, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of an investigational IOL.

NCT ID: NCT01846078 Completed - Cataracts Clinical Trials

Accuracy of Holladay 2 Formula in the Absence of Lens Thickness

Start date: June 2012
Phase: N/A
Study type: Interventional

Hypothesis: Holladay 2 formula is still accurate even used without lens thickness data.

NCT ID: NCT01544777 Completed - Cataract Clinical Trials

Visual Quality Following Aspheric Intraocular Lens (IOL) Implantation - a Comparative Clinical Study

751
Start date: February 2012
Phase: N/A
Study type: Interventional

To evaluate visual acuity and quality of vision in participants undergoing cataract surgery with a Hoya model 751 intra-ocular lens and to compare the visual results to the common monofocal lens in use.

NCT ID: NCT01292629 Completed - Cataract Clinical Trials

Comparison of the Hoya Surgical Optics (HSO) iSert 251 Posterior Chamber Aspheric Aphakic Intraocular Lens to Historical / Literature Controls.

Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this multi-center clinical trail is to determine the safety and efficacy of the iSert 251 for the correction of aphakia.

NCT ID: NCT01268540 Completed - Cataract Clinical Trials

Comparison of Aspheric Toric & Non-toric Aphakic Intraocular Lenses

COAST
Start date: December 2010
Phase: N/A
Study type: Interventional

The purpose of this multi-center clinical trial is to determine the safety and efficacy of the HSO Toric IOLs for the correction of aphakia and reduction of pre-existing refractive astigmatism.

NCT ID: NCT01261975 Completed - Cataract Clinical Trials

Co-Axial Micro-Incision Versus Co-Axial Small Incision Cataract Surgery Using the Stellaris Enhancement System

Start date: August 2009
Phase: Phase 4
Study type: Interventional

The objective of this study is to test the hypothesis that the time to reach a stable refraction is significantly shorter in eyes operated with the 1.8 mm coaxial microincision compared to eyes operated with the 2.75 mm standard incision using the Stellaris Vision Enhancement System.