Clinical Trials Directory

Trials / Completed

CompletedNCT01100411

Changes in Invitro and ex Vivo Lens Metrology With Daily Wear Contact Lenses

Changes in Invitro and ex Vivo Lens Metrology With Experienced Daily Wear Contact Lens Wearers

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
35 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate changes in contact lens geometry after lens wear

Detailed description

The purpose of this study is to evaluate changes invitro and ex vivo in contact lens geometry in daily lens wear

Conditions

Interventions

TypeNameDescription
DEVICEAir Optix AquaContact lens material: Lotrafilcon A
DEVICEBiofinityContact lens material: Comfilcon A
DEVICEProclearContact lens material: Omafilcon A
DEVICEAcuvue OasysContact lens material: Senofilcon A
DEVICEAcuvue 2Contact lens material: Etafilcon A
DEVICEPurevisionContact lens material: Balafilcon A

Timeline

Start date
2010-03-01
Primary completion
2010-07-01
Completion
2010-07-01
First posted
2010-04-09
Last updated
2012-07-18

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT01100411. Inclusion in this directory is not an endorsement.

Changes in Invitro and ex Vivo Lens Metrology With Daily Wear Contact Lenses (NCT01100411) · Clinical Trials Directory