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Clinical Investigation of Omega Refractive Capsule Model V With Use of an FDA Approved IOL — ORCV  

Cataract Clinical Trial

Official title:
Clinical Investigation of Omega Refractive Capsule, Model V in Combination With a Commercially Available, FDA Approved Monofocal or Toric Intraocular Lens

Clinical Trial Summary

The objective of this study is to evaluate the safety and effectiveness of the investigational Omega Refractive Capsule (model V)

Clinical Trial Description

This study is a prospective, interventional, randomized, controlled, paired eye, subject-masked design. Subjects will be randomly assigned to which eye will receive the Omega Refractive capsule V with an FDA approved intraocular lens. Fellow eyes will serve as controls and receive an FDA approved IOL (no Omega capsule). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04574102
Study type Interventional
Source Omega Ophthalmics
Contact
Status Completed
Phase N/A
Start date December 9, 2020
Completion date November 15, 2021
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