The main objective of the clinical study is to evaluate the performance of the CT LUCIA 601
PY for the monocular uncorrected distance visual acuity and compare it to the reference
monofocal IOL Acrysof IQ SN60WF.
Device: Implantation of CT LUCIA IOL
Device: Implantation of Acrysof IQ SN60WF IOL
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Full eligibility criteria for NCT02903927
Ages eligible for Study
50 Years to 90 Years
Genders eligible for Study
Accepts Healthy Volunteers
Patient informed of the consequences and constraints of the protocol and who has given his/her written informed consent;
Patient expected to require retinal laser treatment before the end of the follow-up
Previous intraocular and corneal surgery
Expected postop. astigmatism greater than 1 D
Any type of corneal disorder
Pseudoexfoliation syndrome (PXF)
Glaucoma or IOP higher than 24mmHg under ocular hypertension treatment
Any other pathology or condition presenting, according to the investigator opinion, a risk for the patient
All locations for NCT02903927
View full eligibility
Tris trial is registered with FDA with number: NCT02903927. The sponsor of the trial is Carl Zeiss Meditec AG and it is looking for 81 volunteers for the current phase.
Official trial title: Prospective Comparative Randomized Clinical Trial to Evaluate the Visual Performance of Two Monofocal Intraocular Lenses
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