{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["48(11)"],"submitter":["McCabe C"],"pubmed_abstract":["<h4>Purpose</h4>To evaluate the effectiveness and safety of the DFT015 intraocular lens (IOL) (AcrySof IQ Vivity Extended Vision) compared with an aspheric monofocal control IOL (AcrySof IQ model SN60WF).<h4>Setting</h4>11 investigation sites in the U.S.<h4>Design</h4>Prospective randomized controlled clinical study.<h4>Methods</h4>Patients aged 22 years or older with bilateral cataracts were randomized to receive bilateral implantation of DFT015 or SN60WF. The 4 coprimary effectiveness outcomes (6 months postoperatively) were monocular photopic distance-corrected intermediate visual acuity (DCIVA), monocular photopic corrected distance visual acuity (CDVA), monocular depth of focus (DoF), and the percentage of patients achieving a DCIVA of 0.2 logMAR or better. The mean monocular photopic"],"journal":["Journal of cataract and refractive surgery"],"pagination":["1297-1304"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9622364"],"repository":["biostudies-literature"],"pubmed_title":["Clinical outcomes in a U.S. registration study of a new EDOF intraocular lens with a nondiffractive design."],"pmcid":["PMC9622364"],"pubmed_authors":["Newsom TH","Berdahl J","Reiser H","Lemp-Hull J","McCabe C","Jasti S","Koch D","Cibik L"],"additional_accession":[]},"is_claimable":false,"name":"Clinical outcomes in a U.S. registration study of a new EDOF intraocular lens with a nondiffractive design.","description":"<h4>Purpose</h4>To evaluate the effectiveness and safety of the DFT015 intraocular lens (IOL) (AcrySof IQ Vivity Extended Vision) compared with an aspheric monofocal control IOL (AcrySof IQ model SN60WF).<h4>Setting</h4>11 investigation sites in the U.S.<h4>Design</h4>Prospective randomized controlled clinical study.<h4>Methods</h4>Patients aged 22 years or older with bilateral cataracts were randomized to receive bilateral implantation of DFT015 or SN60WF. The 4 coprimary effectiveness outcomes (6 months postoperatively) were monocular photopic distance-corrected intermediate visual acuity (DCIVA), monocular photopic corrected distance visual acuity (CDVA), monocular depth of focus (DoF), and the percentage of patients achieving a DCIVA of 0.2 logMAR or better. The mean monocular photopic","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Nov","modification":"2025-05-18T11:34:07.166Z","creation":"2024-10-18T02:34:45.406Z"},"accession":"S-EPMC9622364","cross_references":{"pubmed":["35616507"],"doi":["10.1097/j.jcrs.0000000000000978"]}}