Evaluation of a Multi-Purpose Solution

Bausch + Lomb

Status: Completed

Conditions: Contact Lens Solutions

Treatments: Device: Bausch & Lomb Multi-Purpose Solution

Study type: Interventional

Funder types: Industry

Identifiers

NCT00710879

568

Details and patient eligibility

About

This study evaluates a multi-purpose solution when used on a daily wear basis by currently adapted soft contact lens wearers.

Enrollment: 180 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Is an adapted Group I or Group IV soft contact lens wearer and agrees to wear the study lenses on a daily wear basis.
• Must be able and willing to comply with all treatment and follow-up study procedures.
• Must have a clear central cornea.
• VA correctable to 0.3 LogMar or better (driving vision)

Exclusion criteria

• Systemic disease affecting ocular health.
• Using systemic or topical medications.
• Wear monovision, multifocal or toric contact lenses.
• Any grade 2 or greater slit lamp findings.
• Pregnancy

Trial design

Primary purpose: Supportive Care

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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180 participants in 1 patient group

Multipurpose Solution

Experimental group

Description:

Multi-purpose solution administered to adapted FDA group I soft contact lens wearers and FDA group IV soft contact lens wearers.

Treatment:

Device: Bausch & Lomb Multi-Purpose Solution