Not Yet RecruitingPhase 2ACTRN12606000297527

Dispensing evaluation of antibacterial lenses

Evaluation of antibacterial furanone-coated contact lens for safe overnight or daily wear


Sponsor

Institute for Eye Research

Enrollment

200 participants

Start Date

Aug 1, 2006

Study Type

Interventional

Conditions

Summary

To determine whether an antibacterial contact lens can prevent bacterial colonisation of the lens during wear, and can be worn safely. Both the dispensing optometrist and subject wearing lenses will be masked to which lens is being used


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This study investigates Dispensing evaluation of antibacterial lenses. It is looking for both men and women, aged 18 and older who have willing to comply with the wearing and study visit schedule as directed by the investigator;. If you are interested, you may need to attend study visits and follow the research team's instructions.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Comparison of the performance of antibacterial furanone contact lenses to standard marketed highly oxygen permeable contact lenses with overnight wear on a 30 day diposable basis. The study may contin

Comparison of the performance of antibacterial furanone contact lenses to standard marketed highly oxygen permeable contact lenses with overnight wear on a 30 day diposable basis. The study may continue for up to 6 months. Subjects will wear a test antibacterial lens in one eye, and the control marketed lens in the other eye.


Locations(1)

Australia

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ACTRN12606000297527


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