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

N/ACompletedNCT00768885

Bausch & Lomb Incorporated64 enrolled

Overview

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

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SCREENING

Masking

NONE

Enrollment

Conditions

Myopia

Interventions

PureVision 1DEVICE

Currently marketed PureVision soft contact lens.

PureVision 2DEVICE

Alternate design soft contact lens.

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

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.

Locations (1)

Kodama Eye Clinic

Kyoto, Japan

Outcomes

Primary Outcomes

Patient satisfaction

Time frame: 4 weeks

Data from ClinicalTrials.gov

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