Non-comparative Study to Assess the Visual Performances and Safety of a Progressive Multifocal In… (NCT02838004) | Clinical Trial Compass
CompletedNot Applicable
Non-comparative Study to Assess the Visual Performances and Safety of a Progressive Multifocal Intraocular Lens
Germany77 participantsStarted 2016-08
Plain-language summary
This is an interventional, non-controlled, multicenter international trial with a prospective design on one cohort of patients.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.