Non-comparative Study to Assess the Visual Performances and Safety of a Progressive Multifocal Intraocular Lens

An Open Label, Non-comparative Study to Assess the Visual Performances and Safety of a Progressive Multifocal Intraocular Lens With Extended Depth of Focus

This is an interventional, non-controlled, multicenter international trial with a prospective design on one cohort of patients.

To evaluate if the positive results (to assure a good visual acuity at all distances and a good quality of life in terms of glasses independence and absence of undesired events), obtained experimentally using the IOL MINI WELL READY, can be confirmed in the practical surgical routine with a population belonging to different EU countries

Inclusion Criteria:

• Any gender and age above 18 years.
• Refractive lens exchange (RLE) or cataract surgery.
• Healthy corneas, not treated surgically.
• Patients willing to have surgery in both eyes in a short period of time (within 2 weeks).
• Patients request to receive the IOL MINI WELL READY implant

Exclusion Criteria:

• Previous corneal surgery (i.e. pterygium, refractive surgery).
• Eye diseases determining a probable postoperative visual acuity < 20/40.
• Pseudoexfoliation.
• Abnormal pupil size and position.
• Use of contact lens 30 days before the preoperative visit.
• Corneal warpage.
• Predicted postoperative corneal astigmatism higher than 1 D.