[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100651990":3},{"organization":4,"armGroups":7,"interventions":31,"overallOfficials":41,"centralContacts":46,"locations":52,"responsibleParty":66,"collaborators":10,"id":68,"slug":69,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":10,"eligibilityCriteria":74,"healthyVolunteers":75,"sex":76,"minAge":77,"maxAge":10,"enrollmentInfo":78,"targetDuration":10,"studyType":81,"phases":10,"briefSummary":82,"conditions":83,"keywords":85,"overallStatus":91,"whyStopped":10,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":101},{"fullName":5,"class":6},"Alcon Research","INDUSTRY",[8,15,19,23,27],{"label":9,"type":10,"description":11,"interventionNames":12},"Normal Corneas",null,"The eye will be imaged up to seven times with each biometer to achieve three acceptable scans. This cohort will enroll subjects with normal corneas.",[13,14],"Device: UNITY DX","Device: ANTERION",{"label":16,"type":10,"description":17,"interventionNames":18},"Keratoconus","The eye will be imaged up to seven times with each biometer to achieve three acceptable scans. This cohort will enroll subjects with keratoconus.",[13,14],{"label":20,"type":10,"description":21,"interventionNames":22},"Prior Corneal Laser Vision Correction","The eye will be imaged up to seven times with each biometer to achieve three acceptable scans. This cohort will enroll subjects with prior corneal laser vision correction.",[13,14],{"label":24,"type":10,"description":25,"interventionNames":26},"Current and Habitual Contact Lens Wear","The eye will be imaged up to seven times with each biometer to achieve three acceptable scans. This cohort will enroll subjects with current and habitual contact lens wear.",[13,14],{"label":28,"type":10,"description":29,"interventionNames":30},"Dry Eye","The eye will be imaged up to seven times with each biometer to achieve three acceptable scans. This cohort will enroll subjects with dry eye.",[13,14],[32,37],{"type":33,"name":34,"description":35,"armGroupLabels":36,"otherNames":10},"DEVICE","UNITY DX","Investigational non-contact, non-invasive ophthalmic imaging and analysis device used for visualization of ocular structures and their optical properties",[24,28,16,9,20],{"type":33,"name":38,"description":39,"armGroupLabels":40,"otherNames":10},"ANTERION","Commercially available non-contact, non-invasive ophthalmic imaging and analysis device used for visualization of ocular structures and their optical properties",[24,28,16,9,20],[42],{"name":43,"affiliation":44,"role":45},"Clinical Trial Lead, Surgical","Alcon Research, LLC","STUDY_DIRECTOR",[47],{"name":48,"role":49,"phone":50,"phoneExt":10,"email":51},"Alcon Call Center","CONTACT","1-888-451-3937","alcon.medinfo@alcon.com",[53],{"facility":54,"status":10,"city":55,"state":56,"zip":57,"country":58,"countryCode":59,"cosmosGeoPoint":60,"geoPoint":65,"contacts":10},"The Eye Institute of Utah","Salt Lake City","Utah","84107","United States","US",{"type":61,"coordinates":62},"Point",[63,64],-111.89105,40.76078,{"lat":64,"lon":63},{"type":67,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100651990","unity-dx-cornea-study-100651990",false,"NCT07768735","UNITY DX Cornea Study","UNITY DX Cornea Precision and Agreement Study","Key Inclusion Criteria:\n\n* Able to understand and sign an Institutional Review Board approved informed consent form.\n* Willing and able to attend all scheduled study visits as required per protocol.\n* Identified by the investigator as having normal corneas or abnormal corneas per protocol-specified criteria.\n* Other protocol-specified inclusion criteria may apply.\n\nKey Exclusion Criteria:\n\n* Unable to fixate due to nystagmus or other eye movement abnormality, such as significant strabismus.\n* Any ocular disease and\u002For condition that, in the investigator's clinical judgement, may put the subject at significant risk, may compromise study results, or may interfere significantly with the subject's participation in the study.\n* Active ocular infection or inflammation.\n* Other protocol-specified exclusion criteria may apply.",true,"ALL","22 Years",{"count":79,"type":80},110,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to validate the clinical measurement performance of an investigational biometer. Subjects will undergo multiple measurements of the eye, and the agreement, repeatability, and reproducibility of corneal and epithelial thickness maps will be evaluated.",[84],"Tomography",[86,87,88,16,89,90],"Corneal surgery","Refractive surgery","Biometric parameters","Dry eye","Laser vision correction","NOT_YET_RECRUITING","2026-08-12",{"date":94,"type":95},"2026-08-17","ACTUAL",{"date":97,"type":80},"2026-09",{"date":99,"type":80},"2026-12",{"name":5,"class":6},1]