Visual Outcomes After Vivity Toric IOL Implantation

Stopped early · Not applicable

Conditions studied: Refractive Assessment

In brief

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

Key facts

Study ID

NCT04675489

Run by

EVP Eye Care

People needed

4

Starts

2021-01-15

Expected to finish

2021-12-13

Last updated by the study team

2022-01-18

Who can join

Age: 45 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Icon Eye Care — Grand Junction, Colorado, United States

Full record on ClinicalTrials.gov

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