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Sponsored by: |
Alcon Research |
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Information provided by: | Alcon Research |
ClinicalTrials.gov Identifier: | NCT00568386 |
To evaluate drop comfort, acceptability, preference and blur profile between two marketed artificial tears in both dry eye and non-dry eye patient population.
Condition | Intervention |
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Dry Eye |
Other: Systane Lubricant Eye Drops, Optive Lubricant Eye Drops |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Active Control, Crossover Assignment |
Official Title: | Acute Comfort and Blurring Profile Evaluation Comparing Systane Lubricant Eye Drops to Optive Lubricant Eye Drops |
Enrollment: | 40 |
Study Start Date: | November 2007 |
Study Completion Date: | December 2007 |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Responsible Party: | Alcon ( Mike Christensen ) |
Study ID Numbers: | M-07-02 |
Study First Received: | December 5, 2007 |
Last Updated: | December 5, 2007 |
ClinicalTrials.gov Identifier: | NCT00568386 History of Changes |
Health Authority: | United States: Institutional Review Board |
Dry eye |
Pseudoephedrine Oxymetazoline Phenylephrine Vasoconstrictor Agents Ephedrine |
Cardiovascular Agents Peripheral Nervous System Agents Tetrahydrozoline Nasal Decongestants |
Respiratory System Agents Autonomic Agents Sympathomimetics Therapeutic Uses Physiological Effects of Drugs Vasoconstrictor Agents |
Cardiovascular Agents Peripheral Nervous System Agents Tetrahydrozoline Pharmacologic Actions Nasal Decongestants |