Comparative Clinical Evaluation of Daily Disposable Lenses in Symptomatic Frequent Replacement (FRP) Lens Wearers
The trial intends to compare the extent to which symptoms improve in symptomatic daily wear contact lens wearers who replace their lenses at intervals of 2 weeks or monthly when fit with DAILIES AquaComfort Plus versus 1-Day Acuvue TruEye, 1-Day Acuvue Moist, Proclear 1 Day, and SofLens daily disposable worn on a daily wear, daily disposable basis.
Allocation: Randomized, Control: Active Control, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
nelfilcon A with additional UHMW PVA, narafilcon A, etafilcon A, omafilcon A, hilafilcon B
David Wakabayashi, OD
Results (where available)
- Source: http://clinicaltrials.gov/show/NCT00953407
- Information obtained from ClinicalTrials.gov on July 15, 2010
The purpose of this study is to evaluate the performance of the nelfilcon A lens compared to a competitive daily disposable lens, narafilcon A, in a population of neophytes (new wearers).
The primary objective of this trial is to validate the improvements made to the OK inversion indicator. Visibility on eye and on finger will be assessed by the subjects
The objective of this study is to evaluate the clinical performance of two daily disposable contact lenses.
This study seeks to evaluate the clinical fitting performance of a new daily disposable contact lens to an existing daily disposable contact lens.
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.
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Medical and Biotech [MESH] Definitions
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