[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100613087":3},{"organization":4,"outcomesModule":7,"designInfo":30,"detailedDescription":39,"studyPopulation":29,"armGroups":40,"interventions":51,"overallOfficials":60,"centralContacts":64,"locations":72,"responsibleParty":86,"collaborators":29,"id":89,"slug":29,"hasResults":90,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":29,"eligibilityCriteria":94,"healthyVolunteers":90,"sex":95,"minAge":96,"maxAge":97,"enrollmentInfo":98,"targetDuration":29,"studyType":101,"phases":102,"briefSummary":104,"conditions":105,"keywords":107,"overallStatus":110,"whyStopped":29,"lastUpdateSubmitDate":111,"lastUpdatePostDateStruct":112,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":120},{"fullName":5,"class":6},"Vienna Institute for Research in Ocular Surgery","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":29},[9],{"measure":10,"description":11,"timeFrame":12},"Distance-corrected intermediate visual acuity","The difference in distance-corrected intermediate visual acuity before and after surgery will be measured at 66 cm and compared between the two different IOLs","3 months",[14,17,20,23,26],{"measure":15,"description":16,"timeFrame":12},"Uncorrected intermediate visual acuity","The difference in uncorrected intermediate visual acuity before and after surgery will be measured at 66 cm and compared between the two different IOLs",{"measure":18,"description":19,"timeFrame":12},"Corrected and uncorrected distance visual acuity","The difference in corrected and uncorrected distance visual acuity before and after surgery will be measured at 4 m and compared between the two different IOLs",{"measure":21,"description":22,"timeFrame":12},"Corrected and uncorrected near visual acuity","The difference in corrected and uncorrected near visual acuity before and after surgery will be measured at 40 cm and compared between the two different IOLs",{"measure":24,"description":25,"timeFrame":12},"Defocus curve","The difference in visual acuity assessed in the defocus curve before and after surgery and compared between the two different IOLs",{"measure":27,"description":28,"timeFrame":12},"Contrast Sensitivity","The difference in contrast sensitivity between the two different IOLs",null,{"allocation":31,"interventionModel":32,"interventionModelDescription":29,"primaryPurpose":33,"observationalModel":29,"timePerspective":29,"maskingInfo":34},"RANDOMIZED","PARALLEL","TREATMENT",{"masking":35,"maskingDescription":29,"whoMasked":36},"DOUBLE",[37,38],"PARTICIPANT","INVESTIGATOR","Cataracts remain the leading cause of preventable blindness in many developing countries. Over the past decades, cataract surgery has undergone significant advancements. With the development of refined surgical techniques, such as smaller incisions, and the introduction of advanced intraocular lens (IOL) technologies, the procedure has transformed into a refractive approach for visual rehabilitation. The primary goal is to achieve a high level of spectacle independence for patient.\n\nMonofocal lenses are designed with a single fixed focal length and refractive power. While they provide excellent distance vision, patients still need glasses for intermediate and near vision. However, modern patients have increasingly high expectations, often seeking full independence from spectacles after cataract surgery. This growing demand has fueled ongoing research and innovation in the development of advanced IOLs. In contrast, enhanced monofocal IOLs offer optical properties that deliver good intermediate vision outcomes without the negative aspects of multifocal IOLs such as photic phenomena or loss in contrast vision.\n\nThe aim of the study is therefore to compare two refractive enhanced monofocal IOLs in an intra-individual approach.\n\n60 eyes of 30 patients will be included into this study. After randomization one eye is implanted with the Art 25 IOL, whereas the other eye gets the Eyhance IOL. Follow-up visits will be 1 week and 3 months after the surgery.",[41,47],{"label":42,"type":43,"description":44,"interventionNames":45},"Art 25 IOL","EXPERIMENTAL","Patient will receive the Art 25 IOL during cataract surgery",[46],"Device: enhanced monofocal IOL",{"label":48,"type":43,"description":49,"interventionNames":50},"Eyhance","Patient will receive the Eyhance IOL during cataract surgery",[46],[52,57],{"type":53,"name":54,"description":55,"armGroupLabels":56,"otherNames":29},"DEVICE","enhanced monofocal IOL","Art 25 IOL, enhanced monofocal IOL",[42],{"type":53,"name":54,"description":58,"armGroupLabels":59,"otherNames":29},"Eyhance IOL, enhanced monofocal IOL",[48],[61],{"name":62,"affiliation":5,"role":63},"Oliver Findl, Prim. Univ.-Prof. Dr.","PRINCIPAL_INVESTIGATOR",[65,70],{"name":62,"role":66,"phone":67,"phoneExt":68,"email":69},"CONTACT","+43 1 91021","57564","office@viros.at",{"name":71,"role":66,"phone":67,"phoneExt":68,"email":69},"Manuel Ruiss, MSc.",[73],{"facility":5,"status":29,"city":74,"state":29,"zip":75,"country":76,"countryCode":77,"cosmosGeoPoint":78,"geoPoint":83,"contacts":84},"Vienna","1140","Austria","AT",{"type":79,"coordinates":80},"Point",[81,82],16.37208,48.20849,{"lat":82,"lon":81},[85],{"name":62,"role":66,"phone":67,"phoneExt":68,"email":69},{"type":63,"investigatorFullName":87,"investigatorTitle":88,"investigatorAffiliation":5,"oldNameTitle":29,"oldOrganization":29},"Prim. Prof. Dr. Oliver Findl, MBA","Principal Investigator","100613087",false,"NCT07262021","Visual Function of Enhanced Monofocal Intraocular Lenses","Comparison of Visual Function of Enhanced Monofocal Intraocular Lenses After Cataract Surgery","Inclusion Criteria:\n\n* age-related bilateral cataract\n* Age 21 or older\n* Visual acuity \\> 0.05\n* Axial length: 21.00-27.00mm\n* Astigmatism \\\u003C 1.0 dpt\n* Normal findings in the medical history and physical examination\n* Written informed consent prior to surgery\n\nExclusion Criteria:\n\n* Reduced contrast vision, binocularity or stereoscopic vision (e.g. amblyopia, strabismus)\n* Active ocular disease (e.g chronic uveitis, diabetic retinopathy, chronic glaucoma not responsive to medication, corneal dystrophies, etc.) precluding good post- operative visual acuity\n* Relevant other ophthalmic diseases such as pseudoexfoliation syndrome\n* Irregular astigmatism on corneal tomography\n* Pronounced dry eye disease\n* Nystagmus or pathologies that might affect patient's fixation\n* Previous ocular surgery or trauma\n* Persons who are pregnant or nursing","ALL","21 Years","105 Years",{"count":99,"type":100},30,"ESTIMATED","INTERVENTIONAL",[103],"NA","Comparison of the visual function of two enhanced monofocal intraocular lenses after cataract surgery",[106],"Cataract",[106,108,109],"Cataract surgery","intraocular surgery","NOT_YET_RECRUITING","2025-11-21",{"date":113,"type":114},"2025-12-03","ACTUAL",{"date":116,"type":100},"2025-12-01",{"date":118,"type":100},"2027-11-01",{"name":5,"class":6},1]