Fluorophotometry Evaluation of Lubricant Eye Drops

Not Applicable

Completed

• Conditions: Healthy
• Interventions: Other: Refresh Plus Lubricant Eye Drops; Other: Systane Free lubricant eye drops; Other: Visine Tears Lubricant Eye Drops; Other: Refresh Liquigel Lubricant Eye Drops

• Registration Number: NCT00347854
• Lead Sponsor: Alcon Research

Brief Summary

The objective of this study is to evaluate the safety and efficacy of exaggerated use of Lubricant Eye Drops in a population of normal subjects by measuring corneal epithelial permeability to fluorescein.

Detailed Description

Not available

Study Timeline

• Study Start: 2006-04
• Primary Completion: 2006-04
• Study Completion: 2006-04
• Study First Submitted: 2006-06-30
• Study First Submitted QC: 2006-07-03
• Study First Posted: 2006-07-04
• Status Verified: 2012-02
• Last Update Submitted: 2016-11-18
• Last Update Posted: 2016-11-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Ages 18 and over

Exclusion Criteria

• No sodium fluorescein corneal staining at Screening Visit

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Refresh Plus	Refresh Plus Lubricant Eye Drops	-
FID 105783	Systane Free lubricant eye drops	-
Visine	Visine Tears Lubricant Eye Drops	-
Refresh Liquigel	Refresh Liquigel Lubricant Eye Drops	-

Primary Outcome Measures

Name	Time	Method
Epithelial permeability to fluorescein

Secondary Outcome Measures

Name	Time	Method
tear turnover rate

Trial Locations

Locations (1)

Alcon; 🇺🇸 Fort Worth, Texas, United States