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

Not Applicable

Completed

• Conditions: Myopia
• Interventions: Device: PureVision 1; Device: PureVision 2

• Registration Number: NCT00768885
• Lead Sponsor: Bausch & Lomb Incorporated

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2008-09
• Primary Completion: 2008-10
• Study First Submitted: 2008-10-06
• Study First Submitted QC: 2008-10-06
• Study First Posted: 2008-10-08
• Study Completion: 2009-01
• Status Verified: 2013-03
• Last Update Submitted: 2013-03-15
• Last Update Posted: 2013-03-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 64

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
PureVision 1	PureVision 1	PureVision soft contact lens design #1.
PureVision 2	PureVision 2	PureVision soft contact lens design #2

Primary Outcome Measures

Name	Time	Method
Patient satisfaction	4 weeks

Trial Locations

Locations (1)

Kodama Eye Clinic; 🇯🇵 Kyoto, Japan