About this trial
The investigational devices are approved intraocular lenses (IOLs) intended to be implanted after phacoemulsification in individuals suffering from age-related cataract with the need of cataract surgery. Cataract surgery with precedent bilateral randomized IOL implantation will be performed in subjects who have signed an informed consent form. Postoperative examinations will be implemented in accordance with the approved investigational plan.
Eligibility criteria
Qualifiers
Bilateral age-related cataract planned for phacoemulsification extraction and posterior IOL implantation
Age 50 to 100
Visual potential in both eyes of 20/25 or better as determined by investigators estimation
Normal findings in medical history and physical examination unless the investigator considers an abnormality to be clinically irrelevant
Disqualifiers
Preceding intraocular surgery or ocular trauma
Relevant other ophthalmic diseases that particularly effects the zonular apparatus (such as severe pseudoexfoliation syndrome, preceding cryocoagulation, trauma)
Pupil diameter < 2.0 mm (photopic)
Laser treatment
Trial design
Treatments tested in this trial
- phacoemulsification and intraocular lens implantation
- phacoemulsification and intraocular lens implantation
- phacoemulsification and intraocular lens implantation
- phacoemulsification and intraocular lens implantation
- phacoemulsification and intraocular lens implantation
- phacoemulsification and intraocular lens implantation
- phacoemulsification and intraocular lens implantation
- phacoemulsification and intraocular lens implantation
- phacoemulsification and intraocular lens implantation
- phacoemulsification and intraocular lens implantation
Treatment groups
10
Treatment groupsSee each treatment group below.