Active clinical trials for "Myopia"

This study is a masked, multi-center, daily wear, monthly replacement, bilateral, randomized, lens blocked (subjects remain in the same lens brand throughout the study) concurrent control study enrolling up to 90 subjects with a study duration of approximately three months. Subjects will be randomized into the study contact lenses in a two to one (2:1) ratio of fanfilcon A lens (test) to enfilcon A lens (control).

The purpose of this study is to evaluate the performance of two daily disposable contact lenses in a population of neophytes (new wearers).

The purpose of this study was to compare visual performance measures between two multifocal contact lenses on presbyopic wearers.

The purpose of this study is to compare the performance of two commercially marketed contact lenses when worn for up to 4 weeks in a daily wear modality.

The objective of this study is to evaluate the product performance of PureVision2 HD contact lenses.

The purpose of this study is to compare lens surface characteristics and comfort between an experimental contact lens and a marketed contact lens.

The primary objective of this trial is to evaluate the subjective performance of two different daily disposable contact lenses in a population of daily disposable lens wearers.

The objective of this study is to evaluate the performance of the PureVision Lens designs when worn on a 30-day continuous wear basis

The purpose of this trial is to compare two different contact lenses during 4 weeks of wear.

This study seeks to evaluate the clinical performance of a new CE marked daily disposable contact lens that contains a wetting agent to a recently improved daily disposable contact lens.