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Clinical Trial Summary

This is a prospective, multi-centre, randomised, single-blind, cross-over study to compare the BIOFINITY® MULTIFOCAL lens and respectively the AIR OPTIX® AQUA MULTIFOCAL lens (lenses allocated on a ratio of 1/0.5) and the PUREVISION® MULTIFOCAL lens (lenses allocated on a ratio of 1/0.5), in presbyopic patients.


Clinical Trial Description

This is a prospective, multi-centre, randomised, single-blind, cross-over study to compare the BIOFINITY® MULTIFOCAL lens and respectively the AIR OPTIX® AQUA MULTIFOCAL lens (lenses allocated on a ratio of 1/0.5) and the PUREVISION® MULTIFOCAL lens (lenses allocated on a ratio of 1/0.5), in presbyopic patients.

Each subject will have 5 visits with the investigator:

- (V1) An inclusion visit during which the first pair of lenses are fitted;

- (V2) An optimization visit after 7 to 9 days of wearing the first lens;

- (V3) An evaluation visit after an additional 10 to 15 days of wearing the first lens (17 to 24 days) and at which time the second pair of lenses are fitted;

- (V4, V5) Visits are conducted as in V 2 and V3 with the second pair of lenses. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01591499
Study type Interventional
Source Coopervision, Inc.
Contact
Status Completed
Phase N/A
Start date September 2011
Completion date September 2012

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