Two Phase Clinical Study of the Impact of Contact Lenses and Solutions on Corneal Structure

Completed · Not applicable · Has a placebo group

Conditions studied: Normal Contact Lens Wear

In brief

Assess the usefulness of using confocal microscopy to examine changes to the structure of the cornea and to identify any potential consequences of contact lens wear and/or solution use.

Key facts

Study ID

NCT00804999

Run by

Christine Sindt

People needed

51

Starts

2008-11-01

Expected to finish

2009-03-01

Last updated by the study team

2018-01-23

Who can join

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

You may qualify if…

• Vision correctable to 20/30 or better in both eyes
• Successful soft contact lens wear for at least 2 weeks prior to enrollment

You may not qualify if…

• History of hypersensitivity to any of the components in any of the lens solutions
• One functional eye or a monofit lens
• Any abnormal slit-lamp finding at baseline
• Use of topical ocular meds
• Any systemic condition with significant ocular side effects or that interfere with contact lens wear
• Enrollment of the investigator's office staff, relatives or members of their respective households
• Enrollment of more than one member of the same household

Where it is running

• University of Iowa Contact Lens Clinic — Iowa City, Iowa, United States

Full record on ClinicalTrials.gov

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