Masked Comparison of a New PEG Based Artificial Tear and Optive for Comfort, Vision & Wear Time in Patients Wearing Contact Lenses

Completed · Phase 4

Conditions studied: Comfort, Vision and Wear Time

In brief

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.

Key facts

Study ID

NCT00570843

Run by

Bp Consulting, Inc

People needed

50

Starts

2008-03-01

Expected to finish

2010-02-01

Last updated by the study team

2010-02-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• The New York Presbyterian Hospital-Weill Cornell Medical College — New York, New York, United States

Full record on ClinicalTrials.gov

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