Clinical Trials Directory

Trials / Completed

CompletedNCT05226884

Intermediate Vision in Patients With Clareon IOLs Compared to Eyhance IOLs

Status
Completed
Phase
Study type
Observational
Enrollment
310 (actual)
Sponsor
Berkeley Eye Center · Academic / Other
Sex
All
Age
40 Years
Healthy volunteers
Accepted

Summary

Compare visual outcomes in patients with bilateral Clareon Monofocal IOLs versus bilateral Eyhance IOLs.

Detailed description

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 compare distance and intermediate visual acuities and a defocus curve in patients with bilateral Clareon Monofocal IOLs versus bilateral Eyhance IOLs. Patients will be assessed for corrected binocular distance and intermediate vision.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTVisual AcuityMeasurement of distance and intermediate visual acuity at variety targeted correction.
DIAGNOSTIC_TESTDefocus CurveMeasurement of a defocus curve

Timeline

Start date
2021-11-30
Primary completion
2022-08-06
Completion
2022-08-06
First posted
2022-02-07
Last updated
2024-11-15
Results posted
2024-11-15

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05226884. Inclusion in this directory is not an endorsement.