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Prospective Study of an Investigational Daily Disposable Contact Lens

NCT01295905 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2012-07-10

Study results available
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Summary

The purpose of this study is to evaluate the performance of an investigational daily disposable contact lens.

Conditions

  • Myopia

Interventions

DEVICE

narafilcon B contact lens

Commercially marketed silicone hydrogel, single vision soft contact lens

DEVICE

delefilcon A contact lens

Investigational silicone hydrogel, single vision soft contact lens

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2011-05-31
Completion
2011-05-31

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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 NCT01295905 on ClinicalTrials.gov