[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100654292":3},{"organization":4,"outcomesModule":7,"designInfo":13,"detailedDescription":11,"studyPopulation":16,"armGroups":11,"interventions":17,"overallOfficials":11,"centralContacts":11,"locations":22,"responsibleParty":43,"collaborators":11,"id":45,"slug":46,"hasResults":47,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":11,"eligibilityCriteria":50,"healthyVolunteers":51,"sex":52,"minAge":53,"maxAge":11,"enrollmentInfo":54,"targetDuration":57,"studyType":58,"phases":11,"briefSummary":59,"conditions":60,"keywords":11,"overallStatus":25,"whyStopped":11,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},{"fullName":5,"class":6},"Optos, PLC","INDUSTRY",{"primaryOutcomes":8,"secondaryOutcomes":11,"otherOutcomes":11},[9],{"measure":10,"description":11,"timeFrame":12},"Number of images",null,"1 year",{"allocation":11,"interventionModel":11,"interventionModelDescription":11,"primaryPurpose":11,"observationalModel":14,"timePerspective":15,"maskingInfo":11},"OTHER","PROSPECTIVE","Participants with eye disease seen at a US clinical site",[18],{"type":19,"name":20,"description":21,"armGroupLabels":11,"otherNames":11},"DEVICE","imaging device","images captured on a modified P200TE",[23],{"facility":24,"status":25,"city":26,"state":27,"zip":28,"country":29,"countryCode":30,"cosmosGeoPoint":31,"geoPoint":36,"contacts":37},"Bennett & Bloom Eye Centers","RECRUITING","Louisville","Kentucky","40222","United States","US",{"type":32,"coordinates":33},"Point",[34,35],-85.75941,38.25424,{"lat":35,"lon":34},[38],{"name":39,"role":40,"phone":41,"phoneExt":11,"email":42},"Megan Kingdon","CONTACT","(502) 895-0040","megankingdon@eyecarepartners.com",{"type":44,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100654292","modified-p200te-data-collection-100654292",false,"NCT07796230","Modified P200TE Data Collection","Inclusion Criteria\n\nMale or female participants 22 years of age or older who have full legal capacity to volunteer on the date the informed consent is signed\n\nParticipants who can follow the instructions by the clinical staff at the clinical site\n\nParticipants who agree to participate in the study\n\nParticipants with posterior segment eye disease. Example of pathologies may include but are not limited to Age-related macular degeneration, glaucoma, diabetic retinopathy, posterior uveitis, central serous chorioretinopathy, vein occlusion, epiretinal membrane and others as confirmed by the investigator.\n\nExclusion Criteria\n\nParticipants unable to tolerate ophthalmic imaging.\n\nParticipants with ocular media not sufficiently clear to obtain acceptable images.\n\nUnable to obtain acceptable image quality on participant.",true,"ALL","22 Years",{"count":55,"type":56},50,"ESTIMATED","1 Day","OBSERVATIONAL","Images will be collected on the modified P200TE",[61],"Retina Disease","2026-08-27",{"date":64,"type":65},"2026-09-01","ACTUAL",{"date":67,"type":65},"2026-07-29",{"date":69,"type":56},"2026-10-01",{"name":5,"class":6},1]