Evaluation of Corneal Staining With Various Contact Lens/Solution Combinations

Status unconfirmed · Not applicable

Conditions studied: Corneal Epithelial Disruption, Corneal Staining

In brief

The purpose of this study is to quantify the amount of corneal staining observed with various marketed contact lens/multipurpose solution combinations. The hypothesis is that there are measurable differences in the amount of corneal staining between the various combinations.

Key facts

Study ID

NCT00381446

Run by

Andrasko, Gary, OD, LLC

People needed

200

Starts

2005-07-01

Expected to finish

2008-03-01

Last updated by the study team

2007-09-27

Who can join

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

You may qualify if…

• currently wearing soft contact lenses daily wear for at least 2 weeks prior to study
• correct visual acuity of 20/30 or better each eye

You may not qualify if…

• history of hypersensitivity to any components of solution being tested
• any ocular condition prohibiting contact lens wear
• excessive baseline staining as defined in protocol
• use of topical or OTC ocular medications during the study
• seasonal allergies with significant effect on contact lens wear

Where it is running

• Dr. Richard Erdey office — Columbus, Ohio, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.