Intermediate Vision in Patients With Clareon IOLs Compared to Eyhance IOLs

Status Completed

Clinical Trial Summary

This is a non-interventional prospective, comparative study of the outcomes for patients following successful, uncomplicated cataract surgery. All patients will have had bilateral implantation of an Eyhance IOL (DIB00/DIU***) or Clareon IOL (CNA0T0) at the time of uncomplicated cataract surgery. These patients will then be assessed post-operatively to determine binocular intermediate vision. Patients will be assessed for corrected binocular distance and intermediate vision.

Clinical Trial Description

This is a non-interventional prospective, single center, bilateral, non-randomized, open-label, two-arm comparative study of the outcomes for patients following successful, uncomplicated cataract surgery. 155 subjects will be enrolled in each arm of the study, with 310 total subjects. All patients will have had bilateral implantation of an Eyhance IOL (DIB00/DIU***) or Clareon IOL (CNA0T0) at the time of uncomplicated cataract surgery. These patients will then be assessed post-operatively to determine binocular intermediate vision. Patients will be assessed for corrected binocular distance and intermediate vision at plano for the Eyhance group and -0.25D for Clareon group. ;

Study Design

Related Conditions & MeSH terms

Pseudophakia

Clinical Trial Details

NCT number	NCT05226884
Study type	Observational [Patient Registry]
Source	Berkeley Eye Center
Contact
Status	Completed
Phase
Start date	November 30, 2021
Completion date	August 6, 2022

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT01193504` - Randomized, Masked Comparison of Bromfenac and Besifloxacin BID With Either Prednisolone BID or Loteprednol 0.5% BID for Prevention of Retinal Thickening and CME Following Phacoemulsification	Phase 4
Completed	`NCT00347243` - Wavefront Analisys and Contrast Sensitivity of Spherical and Aspherical Intraocular Lenses	Phase 4
Completed	`NCT04208633` - Correlation Between Sulcus Anatomy and Other Parameters After Horizontal & Vertical Intraocular Lens (IOLs) Placements	N/A
Recruiting	`NCT06041139` - Visual Outcomes and Patient Satisfaction With Bilateral PanOptix Verses Bilateral Synergy
Completed	`NCT04533191` - Binocular Custom Vision Utilizing The Light Adjustable Lens (LAL)
Completed	`NCT05735990` - Retrospective Clinical Investigation of the Safety and Performance of 640PM Trifocal IOL Implantation in Patients With Cataract and/or Ametropia (Hyperopia, Myopia) and/or Presbyopia
Recruiting	`NCT04175951` - Tecnis Eyhance Versus Rayner RayOne Study	N/A
Not yet recruiting	`NCT06056154` - Safety and Efficacy of the Hydrophobic Intraocular Lens AsqelioTM Monofocal With Biaspheric Design
Not yet recruiting	`NCT05531110` - Comparison of Two Aspheric Intraocular Lenses for Micro-monovision	N/A
Completed	`NCT01004549` - An Open-Label Evaluation of Degree of Accommodation in Pseudophakic Patients Bilaterally Implanted With Monofocal Intraocular Lenses	N/A
Recruiting	`NCT03823092` - Polarization Perception in Health and Disease. Testing a New Sight Test
Completed	`NCT01310127` - Clinical Outcomes of Bromday (Bromfenac Ophthalmic Solution) 0.09% QD vs. Nevanac (Nepafenac Ophthalmic Suspension) 0.1%	Phase 4
Completed	`NCT05335408` - Evaluation of Visual Function After Bilateral Implantation of EDOF IOLs	N/A
Completed	`NCT05611073` - Maximizing Visual Outcomes With Eyhance IOLs
Completed	`NCT04319497` - Subjective and Objective Refraction in Pseudophakic Patients	N/A
Completed	`NCT05418153` - Synergy Lens Outcomes Evaluation
Recruiting	`NCT06065072` - Comparative Study of the Tomey OA-2000, Tomey CASIA2, and the LenStar LS900
Completed	`NCT02450799` - Corrected VA With Long-Term Follow-Up After AcrySof® Intraocular Lens (IOL) Implantation	N/A
Completed	`NCT00428363` - Effect of Optic Edge Design in a Silicone Intraocular Lens on Posterior Capsule Opacification	Phase 4
Completed	`NCT04468022` - Toric Trifocal IOL Treatment With High Astigmatism and Hyperopia vs SMILE Enhancement After Trifocal IOL Treatment	N/A