Product Preference With Systane Compared to Artificial Tears on Frequency of Drop Use

Not Applicable

Completed

• Conditions: Dry Eye

• Registration Number: NCT00347984
• Lead Sponsor: Alcon Research

Brief Summary

The objective of this study was to evaluate the effect of Systane® compared to marketed artificial tears on the frequency of drop use.

Detailed Description

Not available

Study Timeline

• Study Start: 2005-12
• Primary Completion: 2006-02
• Study Completion: 2006-02
• Study First Submitted: 2006-06-30
• Study First Submitted QC: 2006-07-03
• Study First Posted: 2006-07-04
• Status Verified: 2008-08
• Last Update Submitted: 2012-04-07
• Last Update Posted: 2012-04-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• Subjects age 18 (minimum); reported history of dry eye syndrome in both eyes; TFBUT ≤ 7 seconds in at least 1 eye at Visit 1; ≥ 1+ fluorescein staining score in any region in at least 1 eye at Visit 1; desire to use an artificial tear substitute for dry eye symptoms at least 4 times per day at Visit 1 and Visit 2.

Exclusion Criteria

• Age less than 18 years

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Primary Outcome Measures

Name	Time	Method
Frequency of drop use and/or desire to use; Drop preference

Secondary Outcome Measures

Name	Time	Method
Product questionnaire; Symptoms; Corneal and conjunctival staining; Tear film break-up time (TFBUT).

Trial Locations

Locations (1)

Maryland; 🇺🇸 Andover, Massachusetts, United States