Clinical Trials Logo

Clinical Trial Summary

This is a non-interventional, prospective, observational study of the outcomes for post myopic refractive surgery patients following successful, uncomplicated cataract surgery with bilateral implantation of the Vivity IOL (DAT***/CCWET*). Patients will be assessed for monocular and binocular distance, intermediate, and near vision.


Clinical Trial Description

This is a non-interventional, prospective, single center, bilateral, observational study of the outcomes for 40 post myopic refractive surgery patients following successful, uncomplicated cataract surgery with bilateral implantation of the Vivity IOL (DAT***/CCWET*) performed by 4 surgeons using similar surgical techniques. 40 subjects will be enrolled. Patients will be assessed for monocular and binocular distance, intermediate, and near vision. The hypothesis is that post-refractive patients that have high spherical aberration (SAs) will have excellent outcomes and satisfaction with a Vivity IOL ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06064916
Study type Observational [Patient Registry]
Source Berkeley Eye Center
Contact Diana Hill
Phone 713-620-7640
Email diana.hill@berkeleyeye.com
Status Recruiting
Phase
Start date July 25, 2023
Completion date December 2024

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 NCT05226884 - Intermediate Vision in Patients With Clareon IOLs Compared to Eyhance IOLs
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