Status:
COMPLETED
Product Preference With Systane Compared to Artificial Tears on Frequency of Drop Use
Lead Sponsor:
Alcon Research
Collaborating Sponsors:
ORA, Inc.
Conditions:
Dry Eye
Eligibility:
All Genders
18+ years
Phase:
NA
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.
Eligibility Criteria
Inclusion
- 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
- Age less than 18 years
Key Trial Info
Start Date :
December 1 2005
Trial Type :
INTERVENTIONAL
End Date :
February 1 2006
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT00347984
Start Date
December 1 2005
End Date
February 1 2006
Last Update
April 10 2012
Active Locations (1)
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1
Maryland
Andover, Massachusetts, United States, 01845