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Non-dispense Comfort Comparison of Two Silicone Hydrogel Lenses

NCT00808834 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 196

Last updated 2012-06-29

Study results available
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Summary

The purpose of this study is to compare subjective responses to two contact lenses after 15 minutes of wear.

Conditions

  • Myopia

Interventions

DEVICE

Lotrafilcon A contact lens

Investigational, silicone hydrogel, spherical, soft contact lens

DEVICE

Senofilcon A contact lens

Commercially marketed, silicone hydrogel, spherical, soft contact lens

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

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 NCT00808834 on ClinicalTrials.gov