[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100643061":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":21,"locations":27,"responsibleParty":45,"collaborators":49,"id":53,"slug":54,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":61,"sex":62,"minAge":63,"maxAge":20,"enrollmentInfo":64,"targetDuration":20,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":74,"overallStatus":30,"whyStopped":20,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":85},{"fullName":5,"class":6},"Gordon Schanzlin New Vision","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"DAILIES TOTAL1 Multifocal","EXPERIMENTAL","Participants currently wearing INFUSE One-Day Multifocal (kalifilcon A) are refit into DAILIES TOTAL1 Multifocal (delefilcon A) daily disposable contact lenses and followed for approximately 3 weeks.",[13],"Device: DAILIES TOTAL1 Multifocal (delefilcon A)",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","DAILIES TOTAL1 Multifocal (delefilcon A)","Daily disposable multifocal contact lens refit to match the participant's habitual INFUSE One-Day Multifocal power and add level. Worn a minimum of 8 hours\u002Fday, at least 5 days\u002Fweek for approximately 3 weeks. A mandatory \\~15-minute equilibration period is required before over-refraction at the fitting visit. Power is finalized at Visit 2 if adjustment is needed; the primary endpoint is assessed after 2 weeks on the finalized prescription.",[9],null,[22],{"name":23,"role":24,"phone":25,"phoneExt":20,"email":26},"David Geffen, OD, FAAO","CONTACT","8584556800","dgeffen@gwsvision.com",[28],{"facility":29,"status":30,"city":31,"state":32,"zip":33,"country":34,"countryCode":35,"cosmosGeoPoint":36,"geoPoint":41,"contacts":42},"Gordon Schanzlin New Vision Institute","RECRUITING","La Jolla","California","92037","United States","US",{"type":37,"coordinates":38},"Point",[39,40],-117.2742,32.84727,{"lat":40,"lon":39},[43],{"name":23,"role":24,"phone":44,"phoneExt":20,"email":26},"858-455-6800",{"type":46,"investigatorFullName":47,"investigatorTitle":48,"investigatorAffiliation":5,"oldNameTitle":20,"oldOrganization":20},"PRINCIPAL_INVESTIGATOR","David I Geffen, OD,FAAo","Principal Investigator",[50],{"name":51,"class":52},"Alcon Research","INDUSTRY","100643061","refitting-satisfied-infuse-one-day-multifocal-wearers-to-dailies-total1-multifocal-contact-lenses-100643061",false,"NCT07638943","Refitting Satisfied INFUSE One-Day Multifocal Wearers to DAILIES TOTAL1 Multifocal Contact Lenses","Clinical Outcomes Following Refit From INFUSE One-Day Multifocal to DAILIES TOTAL1 Multifocal in Satisfied Presbyopic Wearers: A Prospective, Open-Label, Single-Arm Study","INFUSETODT1","Inclusion Criteria:\n\nAge ≥40 years at enrollment Current satisfied wearer of Bausch + Lomb INFUSE One-Day Multifocal (kalifilcon A) in both eyes; Contact Lens Dry Eye Questionnaire-8 (CLDEQ-8) score \\\u003C12 at baseline Minimum contact lens wear of ≥8 hours\u002Fday, ≥5 days\u002Fweek, for ≥30 days prior to Visit 1 Best-corrected distance visual acuity ≥20\u002F25 (0.18 LogMAR) or better in each eye Manifest refraction within study lens parameters (Sphere: +6.00 D to -10.00 D; Add: Low, Medium, High) Willing to wear DAILIES TOTAL1 Multifocal lenses for ≥8 hours\u002Fday, ≥5 days\u002Fweek and complete all study questionnaires Able to provide written informed consent and comply with investigator instructions\n\nExclusion Criteria:\n\nActive ocular infection, inflammation, or clinically significant ocular surface disease (e.g., severe dry eye, pterygium, keratoconus) Uncontrolled systemic disease or use of systemic medications known to significantly affect the tear film, unless on a stable dose for ≥90 days History of refractive surgery (LASIK, PRK, RK) or intraocular surgery (cataract or IOL implantation) Clinically significant ectropion, entropion, or trichiasis Baseline corneal fluorescein staining score \\>2 in any single zone (NEI\u002FIndustry scale) Current monovision or modified monovision contact lens wear Pregnant or lactating participants Participation in another clinical trial within 30 days prior to enrollment",true,"ALL","40 Years",{"count":65,"type":66},30,"ESTIMATED","INTERVENTIONAL",[69],"NA","The purpose of this study is to determine the comfort and vision of DAILIES TOTAL1 Multifocal contact lenses in a population of satisfied INFUSE One-Day Multifocal contact lens wearers",[72,73],"Contact Lens Comfort and Successful Refitting","Presbyopia",[75],"contact lenses","2026-06-09",{"date":78,"type":79},"2026-06-11","ACTUAL",{"date":81,"type":79},"2026-05-20",{"date":83,"type":66},"2027-02-28",{"name":5,"class":6},1]