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Active clinical trials for "Myopia"

Results 621-630 of 694

Multi-Centre Clinical Evaluation Of Two Daily Disposable Contact Lenses

Myopia

The purpose of this study is to compare the subjective performance for handling of two daily disposable contact lenses, stenfilcon A and etafilcon A.

Completed21 enrollment criteria

Evaluation of Comfilcon A and Senofilcon A Lenses

Myopia

Evaluation of Comfilcon A and Senofilcon A Lenses

Completed30 enrollment criteria

The Clinical Performance of the Biofinity Contact Lens (Comfilcon A) With Two Lens Care Systems...

Myopia

This will be a controlled and randomized, single-masked, crossover study in which 48 subjects will use the Biofinity Contact Lens (comfilcon A) with each of the two lens care products ('solutions'), (Synergi and Biotrue Multi-purpose Solution) for one month each. Follow-up visits for each solution will take place at one week, two weeks and four weeks: with a one-week 'wash-out' period between the solutions. Key outcome measures for this study include biomicroscopic and subjective responses to the lens/solution combinations.

Completed19 enrollment criteria

BIOCLEAN FIRST CARE EX in Combination With Biofinity Lens

Myopia

To determine if patients are unreactive to the lens care solution / Biofinity combination.

Completed25 enrollment criteria

Product Performance of a Daily Disposable Contact Lens

Myopia

The objective of this one week, single group, bilateral, open-label study is to evaluate the product performance of the Bausch & Lomb daily disposable cosmetic tint contact lens (Test) when worn on a daily disposable basis by adapted current wearers of a marketed opaque tinted soft contact lens.

Completed11 enrollment criteria

Comparison of Lens Fit and Lens Power of a New Contact Lens to Two Marketed Contact Lenses in a...

Myopia

The purpose of this study is to evaluate the comparability of lens fit and lens power of a new contact lens to the lens fit and lens power of two marketed lenses.

Completed17 enrollment criteria

Comparative Study of Two Marketed 1-day Soft Contact Lenses

Myopia

This study is designed to evaluate ocufilcon D lens compared to ocufilcon B lens in a 1-week crossover, daily wear regimen.

Completed22 enrollment criteria

Pilot Evaluation of a New Galyfilcon A Lens Prototype and Enfilcon A Lens

Myopia

The purpose of this study is to compare the visual acuity, limbal and bulbar redness of the new galyfilcon A prototype lenses against Avaira® lenses when worn as daily wear for seven (7) days.

Completed16 enrollment criteria

Feasibility of a New Silicone Hydrogel Lens

Myopia

The objective of this study is to determine the product feasibility of the investigational contact lens (Test) when compared to the currently marketed Acuvue Oasys contact lens (Control) and the Air Optix Aqua contact lens (Control) when worn by adapted wearers of soft contact lenses.

Completed9 enrollment criteria

Product Feasibility of a New Silicone Hydrogel Contact Lens

Myopia

The objective of this study is to determine the clinical feasibility and to evaluate the product performance of investigational contact lens.

Completed7 enrollment criteria
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