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Daily Wear Comparison of Enhanced and Non-Enhanced Silicone Hydrogel Lenses

NCT00813982 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2023-05-26

Study results available
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Summary

The purpose of this study is to compare an experimental contact lens with a currently marketed contact lens.

Conditions

  • Myopia

Interventions

DEVICE

Lotrafilcon A Experimental Contact Lens

Experimental spherical, silicone hydrogel soft contact lens

DEVICE

Lotrafilcon A Commercial Contact Lens

Commercially marketed spherical, silicone hydrogel soft contact lens

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-11-30
Primary Completion
2008-12-31
Completion
2008-12-31

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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 NCT00813982 on ClinicalTrials.gov