Clinical Evaluation of Hydrogels vs Silicone Hydrogel Contact Lenses

NACompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

October 31, 2013

Primary Completion Date

November 30, 2013

Study Completion Date

November 30, 2013

Conditions
Myopia
Interventions
DEVICE

Pair 1 (ocufilcon D / ocufilcon D)

Randomized to contra lateral lens pair 1 (ocufilcon D hydrogel / ocufilcon D hydrogel)

DEVICE

Pair 2 (ocufilcon D / enfilcon A)

Randomized to contra lateral lens pair 2 (ocufilcon D hydrogel / enfilcon A silicone)

DEVICE

Pair 3 (ocufilcon D / comfilcon A)

Randomized to contra lateral lens pair 3 (ocufilcon D hydrogel / comfilcon A silicone)

DEVICE

Pair 4 (methafilcon A / methafilcon A)

Randomized to contra lateral lens pair 4 (methafilcon A hydrogel sphere / methafilcon A hydrogel asphere)

DEVICE

Pair 5 (methafilcon A / comfilcon A)

Randomized to contra lateral lens pair 5 (methafilcon A hydrogel / comfilcon A silicone)

DEVICE

Pair 6 (omafilcon A / comfilcon A)

Randomized to contra lateral lens pair 6 (omafilcon A hydrogel / comfilcon A silicone)

Trial Locations (1)

94720-2020

University of California, Berkeley Clinical Research Center (UCB-CRC), Berkeley

All Listed Sponsors
lead

CooperVision, Inc.

INDUSTRY

NCT01966770 - Clinical Evaluation of Hydrogels vs Silicone Hydrogel Contact Lenses | Biotech Hunter | Biotech Hunter