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ENROLLING BY INVITATION
NCT05729477
NA

A Prospective Multicenter Study To Assess The Clinical Outcomes Of Current Phacoemulsification Approach To Cataract Extraction Versus The Micor System Device

Sponsor: Carl Zeiss Meditec, Inc.

View on ClinicalTrials.gov

Summary

The purpose of this research study is to evaluate the clinical outcomes of current phacoemulsification approaches to cataract extraction involving high-frequency thermogenic energy versus the use of the MICOR System device using low-energy segment removal with a micro-interventional irrigation/aspiration port to evacuate the lens in subjects undergoing routine cataract surgery.

Official title: A Prospective Multicenter Study To Assess The Clinical Outcomes Of Current Phacoemulsification Approach To Cataract Extraction Versus The Micor System Device Using Low Energy Lens Extraction In Patients Undergoing Cataract Surgery

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

375

Start Date

2022-12-06

Completion Date

2026-01

Last Updated

2024-10-17

Healthy Volunteers

Yes

Interventions

DEVICE

miCOR System

The miCOR system is a lens fragmentation device used to break up the cataract prior to IOL implantation during cataract surgery.

DEVICE

Phaco Subject Cohort

Phaco Subject Cohort

Locations (6)

Argus Research at Cape Coral Eye Center

Cape Coral, Florida, United States

Mittleman Eye

West Palm Beach, Florida, United States

Wolfe Eye Clinic

Hiawatha, Iowa, United States

Penn State Health Eye Center

Hershey, Pennsylvania, United States

Virginia Eye Consultants

Norfolk, Virginia, United States

The eye Centers of Racine and Kenosh

Racine, Wisconsin, United States