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Outcomes of a Trifocal IOL in Post-refractive Patients — TrIPLe  

Refractive Errors Clinical Trial

Official title:
Outcomes of a Trifocal IOL in Post-refractive Patients

Clinical Trial Summary

To compare the prediction error of ORA vs formula for post-LASIK cataract patients when PanOptix IOL was implanted. Using post-operative outcomes to determine if preoperative IOL calculations, including Barrett TK, Barrett Universal II, Hill RBF, ASCRS post-refractive calculator, or intraoperative aberrometry is more accurate when the two methods disagree in patients who have had previous refractive surgery undergo cataract surgery.

Clinical Trial Description

The study will be non-interventional with data being collected prospectively and retrospectively between at least two surgical sites. All subjects will have previous LASIK and be at least 3 months post op PanOptix implantation. The study will enroll up to 200 patients and a statistical database will be created. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04545073
Study type Observational
Source Vance Thompson Vision ND
Contact Sarah Thiede
Phone 7015665390
Email sarah.thiede@vancethompsonvision.com
Status Recruiting
Phase
Start date October 9, 2020
Completion date May 2021
View Details
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