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Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Multifocal IOL

NCT02847572 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2017-07-21

No results posted yet for this study

Summary

This will be a single center, non comparison clinical trial. Fifty study patients will have the Symfony IOL implanted in their dominant eye and a +3,25D Tecnis Multifocal in their non-dominant eye. The investigators will be evaluated vision at distance, intermediate and near as well as assessing patient satisfaction and spectacle independence.

Conditions

  • Cataract

Interventions

PROCEDURE

Cataract Surgery

All patients wil be having intraocular lens surgery

Sponsors & Collaborators

  • Abbott

    collaborator INDUSTRY

  • Crystal Clear Vision

    lead OTHER

Principal Investigators

  • Sondra Black, OD · Crystal Clear Vision

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2016-12-31
Completion
2016-12-31

Countries

  • Canada

Study Locations

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Entities

Companies

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 NCT02847572 on ClinicalTrials.gov