Status:

TERMINATED

Visual Outcomes After Vivity Toric IOL Implantation

Lead Sponsor:

EVP Eye Care

Collaborating Sponsors:

Alcon Research

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Conditions:

Refractive Assessment

Eligibility:

All Genders

45+ years

Phase:

NA

Brief Summary

The purpose of this study is to evaluate patient satisfaction after bilateral implantation of Vivity Toric Extended Vision Intraocular lens and visual outcomes.

Detailed Description

To evaluate and report outcomes including postoperative uncorrected visual acuity, postoperative best corrected visual acuity, postoperative refractive error, and IOL rotational stability after Vivity...

Eligibility Criteria

Inclusion

  • Calculated lens power within study IOL range of 15.0 diopters to 25.0 diopters and toric range of T3 to T6
  • Willing and able to comprehend informed consent form and to complete 1 day and 3-4 month postoperative visit
  • Potential postoperative best corrected distance visual acuity of 20/20 or better in each eye based on medical opinion of investigator

Exclusion

  • Ocular pathology or comorbidity that could reduce potential postoperative best corrected distance visual acuity
  • Ocular trauma or zonular weakness/instability
  • Diagnosis of glaucoma or high-risk glaucoma suspect
  • Previous refractive surgery
  • Unreliable preoperative biometry measurements
  • Severe dry eye or ocular surface disease

Key Trial Info

Start Date :

January 15 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 13 2021

Estimated Enrollment :

4 Patients enrolled

Trial Details

Trial ID

NCT04675489

Start Date

January 15 2021

End Date

December 13 2021

Last Update

January 18 2022

Active Locations (1)

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Grand Junction, Colorado, United States, 81501