Clinical Evaluation of an Investigational Soft Contact Lens

Completed · Not applicable

Conditions studied: Myopia

In brief

The purpose of this 4-week dispensing trial is to evaluate and compare an investigational soft contact lens worn on a daily disposable basis with three other soft contact lenses also worn on a daily disposable basis.

Key facts

Study ID

NCT01254747

Run by

CIBA VISION

People needed

130

Starts

2010-11-01

Expected to finish

2010-12-01

Last updated by the study team

2012-07-10

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Germany: Be of legal age.
• USA: Be of legal age or, if under legal age, have written consent of parent/guardian to participate and sign informed assent.
• Sign Informed Consent.
• Wear soft contact lenses for at least 3 months prior to the study.
• Wear soft contact lenses on a daily disposable basis, daily wear basis, or occasional extended wear basis.
• Other protocol-defined inclusion/exclusion criteria may apply.

You may not qualify if…

• Eye injury or surgery within twelve weeks prior to enrollment.
• Pre-existing ocular irritation that would preclude contact lens fitting.
• Currently enrolled in any clinical trial.
• Regularly wear contact lenses on an extended/overnight basis.
• Germany: pregnant or lactating.
• Other protocol-defined inclusion/exclusion criteria may apply.

Where it is running

• CIBA VISION Research Clinic — Duluth, Georgia, United States
• CIBA VISION Research Clinic — Großwallstadt, Germany

Full record on ClinicalTrials.gov

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