A Study to Evaluate the Product Performance of a Low Add MultiFocal Soft Contact Lens

Completed · Not applicable

Conditions studied: Presbyopia

In brief

The objective of this study is to evaluate the product performance of an investigational multifocal low add soft contact lens.

Key facts

Study ID

NCT01539694

Run by

Bausch & Lomb Incorporated

People needed

126

Starts

2012-01-01

Expected to finish

2012-03-01

Last updated by the study team

2020-09-30

Who can join

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

You may qualify if…

• Have physiologically normal anterior segments.
• Be adapted wearers of soft contact lenses and wear a lens in each eye.
• Be presbyopic and require near add correction in each eye.
• Have no active ocular disease or allergic conjunctivitis.
• Must not be using any topical ocular medications.

You may not qualify if…

• Any Grade 2 or greater finding during the slit lamp examination.
• Any scar or neovascularization within the central 4mm of the cornea.
• Any "Present" finding during the slit lamp examination that, in the Investigator's judgment, interferes with contact lens wear.
• Allergic to any component in the study products.
• Any systemic disease affecting ocular health.
• Using any systemic or topical medications that will affect ocular physiology or lens performance.
• An active ocular disease, any corneal infiltrative response or are using any ocular medications.

Where it is running

• Bausch & Lomb Incorporated — 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.