Comparison of 3 Novel Contact Lens Solutions on the Basal Lamina

Not Applicable

Completed

• Conditions: Contact Lens Solution
• Interventions: Device: Opti-Free contact lens solution; Device: ReNu Multiplus contact lens solution; Device: Clear Care contact lens solution

• Registration Number: NCT00691457
• Lead Sponsor: Alcon Research

Brief Summary

Three arm study comparing three novel contact lens solutions.

Detailed Description

Not available

Study Timeline

• Study Start: 2008-04
• Study First Submitted: 2008-06-03
• Study First Submitted QC: 2008-06-04
• Study First Posted: 2008-06-05
• Primary Completion: 2009-01
• Study Completion: 2009-01
• Status Verified: 2009-06
• Last Update Submitted: 2012-09-28
• Last Update Posted: 2012-10-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	Opti-Free contact lens solution	Opti-Free contact lens solution
2	ReNu Multiplus contact lens solution	ReNu Multiplus contact lens solution
3	Clear Care contact lens solution	Clear Care contact lens solution

Primary Outcome Measures

Name	Time	Method
Change from baseline in corneal fluorescein staining as evaluated at Day 30	30 Days

Secondary Outcome Measures

Name	Time	Method
Confocal evaluation variables as measured at Days 0, 14, and 30	Day 0, 14, 30

Trial Locations

Locations (1)

Virginia Beach, VA; 🇺🇸 Virginia Beach, Virginia, United States