Clinical Trials Directory

Trials / Completed

CompletedNCT01966770

Clinical Evaluation of Hydrogels vs Silicone Hydrogel Contact Lenses

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
CooperVision, Inc. · Industry
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

The aim of this fitting study is to evaluate the clinical performance of different hydrogel and silicone hydrogel contact lenses.

Detailed description

This is a 20-subject, double masked, randomized, contra lateral, 2-day non-dispensing fitting trial.

Conditions

Interventions

TypeNameDescription
DEVICEPair 1 (ocufilcon D / ocufilcon D)Randomized to contra lateral lens pair 1 (ocufilcon D hydrogel / ocufilcon D hydrogel)
DEVICEPair 2 (ocufilcon D / enfilcon A)Randomized to contra lateral lens pair 2 (ocufilcon D hydrogel / enfilcon A silicone)
DEVICEPair 3 (ocufilcon D / comfilcon A)Randomized to contra lateral lens pair 3 (ocufilcon D hydrogel / comfilcon A silicone)
DEVICEPair 4 (methafilcon A / methafilcon A)Randomized to contra lateral lens pair 4 (methafilcon A hydrogel sphere / methafilcon A hydrogel asphere)
DEVICEPair 5 (methafilcon A / comfilcon A)Randomized to contra lateral lens pair 5 (methafilcon A hydrogel / comfilcon A silicone)
DEVICEPair 6 (omafilcon A / comfilcon A)Randomized to contra lateral lens pair 6 (omafilcon A hydrogel / comfilcon A silicone)

Timeline

Start date
2013-10-01
Primary completion
2013-11-01
Completion
2013-11-01
First posted
2013-10-22
Last updated
2020-07-30
Results posted
2015-02-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01966770. Inclusion in this directory is not an endorsement.