Evaluation of Deposits on Contact Lenses Worn Extended Wear

Completed · Not applicable

Conditions studied: Myopia

In brief

The purpose of this study was to measure lipid deposits on commercially marketed contact lenses when worn on an extended wear (overnight) basis for 7 days.

Key facts

Study ID

NCT00725530

Run by

Alcon Research

People needed

54

Starts

2008-03-01

Expected to finish

2008-10-01

Last updated by the study team

2012-08-22

Who can join

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

You may qualify if…

• Age 18 or older.
• Visual acuity correctable to 20/30 (Snellen) or better in each eye at distance with contact lenses.
• Successfully wearing hydrogel or silicone hydrogel contact lenses.
• Other protocol-defined inclusion criteria may apply.

You may not qualify if…

• Evidence or history of ocular conditions as prescribed in the protocol.
• One functional eye or a monofit lens.
• Any slit-lamp finding score of (1) at the Screening Visit as defined by the protocol.
• Use of concomitant topical ocular prescription or over-the-counter ocular medications.
• History of seasonal allergies with significant ocular side effects.
• 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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