Product Preference With Systane Compared to Artificial Tears on Frequency of Drop Use
Completed · Not applicable
Conditions studied: Dry Eye
In brief
The objective of this study was to evaluate the effect of Systane® compared to marketed artificial tears on the frequency of drop use.
Key facts
- Study ID
- NCT00347984
- Run by
- Alcon Research
- People needed
- 50
- Starts
- 2005-12-01
- Expected to finish
- 2006-02-01
- Last updated by the study team
- 2012-04-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- Age less than 18 years
Where it is running
- Maryland — Andover, Massachusetts, United States
Full record on ClinicalTrials.gov
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