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OpenTrials
Completed

NCT Number: NCT00691457

Comparison of 3 Novel Contact Lens Solutions on the Basal Lamina

Three arm study comparing three novel contact lens solutions.

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Key information

Conditions

Contact Lens Solution

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Virginia Beach, VA

Virginia Beach, Virginia, 23462, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion:

  • Stable distance contact lens prescription between -0.50 D and 9.00 D and astigmatism less than or equal to -1.00 D cylindrical (cyl).
  • Stable correction is defined as longer than six months.
  • Worn a single brand of disposable silicone hydrogel contact lenses successfully (i.e., without complications or discomfort) for a minimum of six months

Exclusion:

  • Known sensitivity to the contact lens disinfecting solutions or fluorescein dye.
  • Any systemic or ocular disease that could affect contact lens wear.
  • Women who are pregnant or lactating.

Treatment and study plan

Opti-Free contact lens solution

Device

Solution

ReNu Multiplus contact lens solution

Device

Solution

Clear Care contact lens solution

Device

Solution

Primary outcomes

  1. Change from baseline in corneal fluorescein staining as evaluated at Day 30

    Time frame: 30 Days

Secondary outcomes

  1. Confocal evaluation variables as measured at Days 0, 14, and 30

    Time frame: Day 0, 14, 30

Sponsors and collaborators

Lead sponsor

Alcon Research

Industry

Registry information

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Jun 5, 2008
Registry last updated
Oct 1, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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