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Clinical Evaluation of Two Daily Disposable Lenses in Neophytes

NCT00987623 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 326

Last updated 2012-07-10

Study results available
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Summary

The purpose of this study is to evaluate the performance of two daily disposable contact lenses in a population of neophytes (new wearers).

Conditions

  • Myopia

Interventions

DEVICE

nelfilcon A contact lens

Commercially marketed, hydrogel, single-vision contact lens for daily wear, daily disposable use.

DEVICE

narafilcon A contact lens

Commercially marketed, silicone hydrogel, single-vision contact lens for daily wear, daily disposable use.

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Max Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-08-31
Primary Completion
2009-12-31
Completion
2009-12-31

Countries

  • United States

Study Locations

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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 NCT00987623 on ClinicalTrials.gov