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Comparison of Two Multifocal Contact Lenses

NCT01250054 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 17

Last updated 2012-06-29

Study results available
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Summary

The purpose of this study is to compare two multifocal contact lenses in presbyopic wearers.

Conditions

Interventions

DEVICE

Lotrafilcon B contact lens

Commercially marketed, silicone hydrogel, multifocal contact lens for daily wear use

DEVICE

Comfilcon A contact lens

Commercially marketed (Europe), silicone hydrogel, multifocal contact lens for daily wear use

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
35 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-10-31
Primary Completion
2010-10-31
Completion
2010-10-31

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Entities

Diseases

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 NCT01250054 on ClinicalTrials.gov