Presbyopia Clinical Trial
Official title:
Clinical Evaluation of the Biofinity Multifocal Lens Compared With the Air Optix Aqua Multifocal Lens and With PureVision Multifocal Lens (INNOVATION PRESBYOPIA Study)
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.
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.
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