The study is a prospective randomised controlled study. The patients get monolateral IOL implantation of POD F GF and POD F in the contralateral eye. Both IOLs are trifocal IOLs consisting of the same optical design. The difference between the IOLs is the material (hydrophilic and hydrophobic). To decide which eye receives POD F and which eye receives POD F GF, a randomization table will be provided to the principle investigator.
The examinations consist of visual acuity data, contrast sensitivity exams and slitlamp examinations. Follow up will be up to 6 months postoperative.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
25
Implantation of trifocal IOL POD F GF consisting of hydrophobic material
Implantation of trifocal IOL POD F consisting of hydrophilic material
Semmelweis University - Department of Ophthalmology
Budapest, Hungary
Visual Acuity at far, near and intermediate distance
ability to read letters at different distances
Time frame: 6 months postoperative
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