Clinical Trials Directory

Trials / Completed

CompletedNCT01684046

Evaluation of the Effectiveness of Two Marketed Multi-Purpose Solutions for Silicone Hydrogel Contact Lenses - Study 2

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
196 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to evaluate the performance of Opti-Free® PureMoist® Multi-purpose Disinfecting Solution (MPDS) compared to AMO RevitaLens OcuTec® MPDS (US brand name)/COMPLETE RevitaLens (Europe brand name) in silicone hydrogel contact lens wearers.

Detailed description

In this 2-period crossover study, eligible participants were randomized to either Opti-Free® PureMoist MPDS or RevitaLens MPDS in Period 1 for use with their habitual contact lenses, after which they switched to the alternate solution in Period 2. Each period was 30 days in length. A 2-day washout period during which participants refrained from using a multi-purpose contact lens solution preceded Period 1 and Period 2.

Conditions

Interventions

TypeNameDescription
DEVICEOpti-Free® PureMoist® MPDS
DEVICERevitaLens MPDS
DEVICEHabitual Contact LensesSilicone hydrogel contact lenses per participant's habitual brand, prescription, and replacement schedule worn on a daily wear basis for at least 8 hours a day, 5 days a week for the duration of the study. During the washout period, the contact lenses were worn on a daily disposable basis.

Timeline

Start date
2012-11-01
Primary completion
2013-03-01
Completion
2013-03-01
First posted
2012-09-12
Last updated
2014-04-29
Results posted
2014-04-29

Source: ClinicalTrials.gov record NCT01684046. Inclusion in this directory is not an endorsement.