[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100585207":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":12,"centralContacts":17,"locations":22,"responsibleParty":39,"collaborators":10,"id":41,"slug":42,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":43,"sex":49,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":10,"studyType":55,"phases":10,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":25,"whyStopped":10,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":72},{"fullName":5,"class":6},"University of Udine","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":10},"Observational cohort of patients with age-related macular degeneration",null,"Observational cohort of patients with age-related macular degeneration eventually receiving anti-VEGF agents as per clinical practice.",[13],{"name":14,"affiliation":15,"role":16},"Daniele Veritti","Department of Ophthalmology, University of Udine","PRINCIPAL_INVESTIGATOR",[18],{"name":14,"role":19,"phone":20,"phoneExt":10,"email":21},"CONTACT","+390432559907","daniele.veritti@uniud.it",[23],{"facility":24,"status":25,"city":26,"state":27,"zip":28,"country":29,"countryCode":30,"cosmosGeoPoint":31,"geoPoint":36,"contacts":37},"Department of Ophthalmology","RECRUITING","Udine","UD","33100","Italy","IT",{"type":32,"coordinates":33},"Point",[34,35],13.23715,46.0693,{"lat":35,"lon":34},[38],{"name":14,"role":19,"phone":20,"phoneExt":10,"email":21},{"type":16,"investigatorFullName":14,"investigatorTitle":40,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"Prof.","100585207","evaluation-of-clinical-progression-prognostic-factors-and-quality-of-life-in-patients-with-age-related-macular-degeneration-100585207",false,"NCT06899360","Evaluation of Clinical Progression, Prognostic Factors, and Quality of Life in Patients with Age-related Macular Degeneration.","Evaluation of Clinical Progression, Prognostic Factors, and Quality of Life in Patients with Age-related Macular Degeneration (VERA-nAMD).","VERA-AMD","Inclusion Criteria:\n\n* age ≥ 50 years.\n* confirmed diagnosis of AMD in at least one eye.\n* follow-up scheduled according to standard clinical practice.\n\nExclusion Criteria:\n\n* presence of other significant ocular conditions that could affect visual acuity.\n* systemic conditions that make the patient unsuitable for long-term follow-up.","ALL","50 Years","120 Years",{"count":53,"type":54},200,"ESTIMATED","OBSERVATIONAL","The VERA-AMD study is a prospective, observational study designed to evaluate clinical progression, prognostic factors, and quality of life in patients with age-related macular degeneration (AMD). The study aims to analyze real-world clinical data to identify key predictors of disease progression and functional outcomes, with the goal of optimizing AMD management. The study involves 200 patients aged ≥50 with a confirmed diagnosis of AMD, monitored through routine clinical practice. Primary outcomes include progression rates to advanced AMD and changes in visual acuity, while secondary outcomes focus on retinal morphology and quality of life. Anti-VEGF therapy and AI-based fluid analysis will be integrated to explore their impact on disease progression and patient outcomes.",[58],"Age-Related Macular Degeneration",[60,61,62],"age-related macular degeneration","artificial intelligence","anti-VEGF","2025-03-20",{"date":65,"type":66},"2025-03-27","ACTUAL",{"date":68,"type":66},"2024-10-01",{"date":70,"type":54},"2029-10-01",{"name":5,"class":6},1]