Expired Study
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New York, New York 10021


Purpose:

The objective of this study is to evaluate the effect of a new PEG based artificial tear as compared to Optive on comfort, wear time, and vision in patients wearing contact lenses.


Criteria:

Inclusion Criteria: - Use of soft contact lenses (e.g. silicone hydrogel lenses, daily disposables etc.) and multipurpose solution for cleaning, including enzyme-based cleaners (ClearCare etc.) - Able to wear contact lenses for approximately 10-12 hours/day - Willingness to complete entire length of trial and comply with subjective questionnaire. Exclusion Criteria: - Patients taking topical cyclosporine (Restasis) - Patients currently using Optive for dryness relief. - Patients wearing hard or rigid gas permeable lenses - Patients with uncontrolled systemic disease which may confound the results of the trial.


NCT ID:

NCT00570843


Primary Contact:

Principal Investigator
Chris Starr, MD
The New York Presbyterian Hospital Weill Cornell Medical College


Backup Contact:

N/A


Location Contact:

New York, New York 10021
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 19, 2017

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