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Subjective Evaluation of a Commercially Marketed Contact Lens Amongst a Subset of the Contact Lens Wearing Population

NCT01007916 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2012-07-10

Study results available
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Summary

The purpose of this study is to compare the performance of commercially marketed contact lenses to habitual contact lenses in a selected segment of the contact lens wearing population.

Conditions

  • Myopia

Interventions

DEVICE

Lotrafilcon B contact lens

Commercially marketed, silicone hydrogel, spherical contact lens having a recommended replacement schedule of monthly.

DEVICE

Habitual contact lens

Habitual soft spherical contact lens having a recommended replacement schedule of 2 weeks or monthly.

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2010-01-31
Completion
2010-01-31

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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 NCT01007916 on ClinicalTrials.gov