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Comparison of 3 Novel Contact Lens Solutions on the Basal Lamina

Comparison of 3 Novel Contact Lens Solutions on the Basal Lamina

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00691457
Enrollment
15
Registered
2008-06-05
Start date
2008-04-30
Completion date
2009-01-31
Last updated
2012-10-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Contact Lens Solution

Keywords

Contact lens, solution, confocal microscope

Brief summary

Three arm study comparing three novel contact lens solutions.

Interventions

DEVICEOpti-Free contact lens solution

Solution

DEVICEReNu Multiplus contact lens solution

Solution

DEVICEClear Care contact lens solution

Solution

Sponsors

Alcon Research
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Change from baseline in corneal fluorescein staining as evaluated at Day 3030 Days

Secondary

MeasureTime frame
Confocal evaluation variables as measured at Days 0, 14, and 30Day 0, 14, 30

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026