Performance Evaluation of Contact Lenses Among a Population of Adapted Contact Lens Wearers

Completed · Not applicable

Conditions studied: Vision Disorders

In brief

This study is being conducted to evaluate Bausch \& Lomb PureVision Multi-Focal contact lenses compared to the Bausch \& Lomb SofLens59 contact lens when worn by adapted soft contact lens wearers on a daily wear basis.

Key facts

Study ID

NCT00985231

Run by

Bausch & Lomb Incorporated

People needed

272

Starts

2009-09-01

Expected to finish

2009-12-01

Last updated by the study team

2015-03-24

Who can join

Age: 30 and older, up to 40. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects must have clear central corneas and be free of any anterior segment disorders.
• Subjects must be adapted soft contact lens wearers and agree to wear the study lenses on a daily wear basis for at least eight hours a day for approximately two weeks.
• Subjects must wear a lens in each eye and each lens must be of the same manufacture and brand.

You may not qualify if…

• Subjects participating in any drug or device clinical investigation within two weeks prior to entry into this study and/or during the period of study participation.
• Subjects with any systemic disease affecting ocular health
• Subjects with an active ocular disease or using any ocular medication.
• Subjects who have had any corneal surgery (eg, refractive surgery).

Where it is running

• Bausch & Lomb — Rochester, New York, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.