Vistakon Investigational Multi-purpose Contact Lens Care Solution.

Johnson & Johnson (J&J)

Status: Completed

Conditions: Contact Lens Wear

Treatments: Device: ReNu MultiPlus Multi-Purpose Solution; Device: Vistakon Investigational Multi-Purpose Solution II

Study type: Interventional

Funder types: Industry

Identifiers

NCT01055457

CR-1650

Details and patient eligibility

About

This study compares an investigational contact lens care multi-purpose solution to a currently marketed multi-purpose solution.

Enrollment: 315 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• must be an adapted contact lens wearer
• best corrected distance visual acuity must be 20/25 or better in each eye
• must be wearing their habitual lenses on a daily wear basis
• must be willing to refrain from swimming during the study

Exclusion criteria

• any systemic diseases that may interfere with contact lens wear
• any clinically significant ocular disease
• any ocular infection
• use of certain medications
• any grade 2 or greater slit lamp findings
• any know sensitivity to marketed contact lens care solutions
• currently pregnant or lactating
• monovision corrected

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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315 participants in 2 patient groups

Experimental Multi-Purpose Solution

Experimental group

Description:

contact lens care solution

Treatment:

Device: Vistakon Investigational Multi-Purpose Solution II

ReNu MultiPlus Multi-Purpose Solution

Active Comparator group

Description:

contact lens care solution

Treatment:

Device: ReNu MultiPlus Multi-Purpose Solution