MedTrace Logo

Clinical Study to Evaluate the Visual Performance of Three Multifocal IOLs

NCT02990689 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 55

Last updated 2018-09-06

No results posted yet for this study

Summary

The purpose of this study is to compare the performances of 2 bifocal IOLs and 1 trifocal IOL for far, near and intermediate vision.

Conditions

  • Visual Acuity

Interventions

DEVICE

Trifocal Intraocular Lens

bifocal intraocular lens (IOL)

DEVICE

Bifocal Intraocular Lens

trifocal intraocular lens (IOL)

DEVICE

Low Addition Bifocal Intraocular Lens

low near addition intraocular lens (IOL)

Sponsors & Collaborators

  • Carl Zeiss Meditec AG

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2015-04-30
Completion
2015-10-31

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02990689 on ClinicalTrials.gov