Active clinical trials for "Myopia"

This is a study to evaluate the performance of fanfilcon A lens when worn on a daily wear modality over approximately 1 month in comparison to the lotrafilcon B lens.

This study is to investigate whether novel soft contact lens optical designs can slow myopia progression.

This study is being conducted to evaluate the product performance of SofLens daily disposable contact lenses packaged in an investigational Test solution versus SofLens daily disposable contact lenses packaged in the currently marketed solution (Control), as it relates to comfort when worn by adapted soft contact lens wearers on a daily-wear basis.

The purpose of this study is to evaluate the performance of an investigational daily disposable contact lens.

This purpose of this study is to compare the clinical performance and subjective acceptance of two different daily disposable limbal ring lenses.

The primary objective of the study was to investigate current criteria driving re-treatment in patients affected by Choroidal Neovascularization (CNV) secondary to Pathologic Myopia (PM) and experiencing a relapse of the disease after the first administration of ranibizumab.

The objective of this study is to compare the clinical performance of ProClear 1-Day versus 1-Day Acuvue Moist each for one week of daily disposable wear.

The purpose of this study is to compare the amount of coma as measured by aberrometry induced by two silicone hydrogel toric lenses in astigmatic participants.

To evaluate the clinical performance of daily disposable etafilcon A lenses.

The purpose of this 3-month study is to evaluate subjective responses to an upgraded contact lens.