Acute Comfort and Blur of Systane Ultra and Systane

Not Applicable

Completed

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

• Registration Number: NCT00748865
• Lead Sponsor: Alcon Research

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2008-07
• Primary Completion: 2008-08
• Study Completion: 2008-08
• Study First Submitted: 2008-09-05
• Study First Submitted QC: 2008-09-05
• Study First Posted: 2008-09-09
• Results First Submitted: 2009-09-25
• Results First Submitted QC: 2010-02-23
• Results First Posted: 2010-03-11
• Status Verified: 2012-01
• Last Update Submitted: 2012-01-31
• Last Update Posted: 2012-02-02

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Documented diagnosis of dry eye

Exclusion Criteria

• Use of contact lens within 7 days preceding enrollment

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

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

Primary Outcome Measures

Name	Time	Method
Drop Comfort	once upon instillation	Drop comfort grading scale is a 0 to 9 scale, with 0 meaning most comfortable and 9 meaning most uncomfortable,

Trial Locations

Locations (1)

Contact Alcon Call Center for Trial Location; 🇺🇸 Fort Worth, Texas, United States