Acute Comfort and Blur of Systane and Optive

Not Applicable

Completed

• Conditions: Dry Eye
• Interventions: Other: Optive Lubricant Eye Drops; Other: Systane Lubricant Eye Drops

• Registration Number: NCT00568386
• Lead Sponsor: Alcon Research

Brief Summary

To evaluate drop comfort, acceptability, preference and blur profile between two marketed artificial tears in both dry eye and non-dry eye patient population.

Detailed Description

Not available

Study Timeline

• Study Start: 2007-11
• Study Completion: 2007-12
• Study First Submitted: 2007-12-05
• Study First Submitted QC: 2007-12-05
• Study First Posted: 2007-12-06
• Results First Submitted: 2008-12-18
• Results First Submitted QC: 2010-02-23
• Results First Posted: 2010-03-10
• Status Verified: 2012-01
• Last Update Submitted: 2012-01-31
• Last Update Posted: 2012-02-02

Recruitment & Eligibility

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

Inclusion Criteria

• Healthy, normal eyes OR documented diagnosis of dry eye

Exclusion Criteria

• Must not have worn contact lenses for 7 days preceding enrollment

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Optive Lubricant Eye Drops	Optive Lubricant Eye Drops	Optive Lubricant Eye Drops 1 drop each one time
Systane Lubricant Eye Drops	Systane Lubricant Eye Drops	Systane Lubricant Eye Drops 1 drop in each eye one time

Primary Outcome Measures

Name	Time	Method
Visual Blur	3 minutes post dose	Visual blur profile is a visual scale ranging from 0 (no blur) to 50 (most blurry). Patients were asked to rate there vision on a specific focal point (an object in the room) through 3 minutes.