Evaluation of Contact Lenses and Conjunctival Staining in Normal Patients

Completed · Not applicable

Conditions studied: Conjunctival Staining

In brief

The purpose of this study was to investigate contact lens fit, lens parameters, and conjunctival staining in a sample of subjects with various contact lens/solution combinations.

Key facts

Study ID

NCT00799422

Run by

Alcon Research

People needed

26

Starts

2008-11-01

Expected to finish

2009-03-01

Last updated by the study team

2012-11-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Successfully wearing hydrogel and/or silicone hydrogel contact lenses;
• Read, sign, and date informed consent/HIPAA document;
• Vision correctable to 20/30 (Snellen) or better in each eye at distance with habitual spectacles;
• Willing and able to discontinue contact lens wear when requested during the study;
• Other protocol-defined inclusion criteria may apply.

You may not qualify if…

• Evidence or history of ocular disease or pathology;
• One functional eye or a monofit lens;
• Use of concomitant topical ocular prescription or over-the-counter ocular medications;
• History of seasonal allergies with significant ocular side effects which may have an adverse impact on contact lens wear;
• Other protocol-defined exclusion criteria may apply.

Where it is running

• Alcon Call Center for Trial Locations — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

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