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Sponsors and Collaborators: |
Alcon Research Ophthalmic Research Associates |
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Information provided by: | Alcon Research |
ClinicalTrials.gov Identifier: | NCT00347984 |
The objective of this study was to evaluate the effect of Systane® compared to marketed artificial tears on the frequency of drop use.
Condition | Intervention |
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Dry Eye |
Drug: Systane Lubricant eye drops |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Active Control, Crossover Assignment, Safety/Efficacy Study |
Official Title: | The Effect of Systane® Compared to Marketed Artificial Tears on Frequency of Drop Use |
Estimated Enrollment: | 50 |
Study Start Date: | December 2005 |
Study Completion Date: | February 2006 |
Primary Completion Date: | February 2006 (Final data collection date for primary outcome measure) |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United States, Massachusetts | |
Maryland | |
Andover, Massachusetts, United States, 01845 |
Study Director: | Mike Christensen | Alcon Research |
Study ID Numbers: | 05-004-09 |
Study First Received: | June 30, 2006 |
Last Updated: | August 4, 2008 |
ClinicalTrials.gov Identifier: | NCT00347984 |
Health Authority: | United States: Institutional Review Board |
Lacerations Tetrahydrozoline |