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Evaluation of Silicone Hydrogel Lens Wettability With Marketed Lens Care Solutions

NCT01252134 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2012-06-11

Study results available
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Summary

The purpose of this study is to assess ex vivo wettability of a commonly prescribed silicone hydrogel (SiH) contact lens with three marketed contact lens care solutions.

Conditions

  • Contact Lens Wear

Interventions

DEVICE

Biotrue multipurpose solution

Contact lens care solution

DEVICE

Sauflon Synergi multipurpose solution

Contact lens care solution

DEVICE

OTE Elements multipurpose solution

Contact lens care solution

DEVICE

Silicone hydrogel contact lenses (Acuvue Advance)

Commercially marketed contact lenses

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-11-30
Primary Completion
2011-02-28
Completion
2011-02-28

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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 NCT01252134 on ClinicalTrials.gov