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

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