Comparative Study of the Wearing Satisfaction of Two Soft Contact Lens Designs.

Bausch + Lomb

Status: Completed

Conditions: Myopia

Treatments: Device: PureVision 1; Device: PureVision 2

Study type: Interventional

Funder types: Industry

Identifiers

NCT00768885

MDPTLD0809

Details and patient eligibility

About

To evaluate the wearing satisfaction of a new design of the PureVision soft contact lenses.

Enrollment: 64 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Subject is myopic
• Subjects who wear soft contact lenses that are exchanged at least biweekly at the time consent is obtained.

Exclusion criteria

• Systemic disease affecting ocular health
• Using pharmaceuticals that may affect the function of the eyes or lenses.
• Subject possessing corneal infiltrate or corneal ulcers.

Trial design

Primary purpose: Screening

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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64 participants in 2 patient groups

PureVision 1

Active Comparator group

Description:

PureVision soft contact lens design #1.

Treatment:

Device: PureVision 1

PureVision 2

Experimental group

Description:

PureVision soft contact lens design #2

Treatment:

Device: PureVision 2