EICHORCondition: Myopia · Sponsor: Santen SAS
Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.
This study aims to assess the impact of myopia in childhood and its long-term complications in adulthood on health-related Quality of Life (HRQoL), providing valuable data for cost-effectiveness models. It will gather country-specific information on healthcare resource utilization, including treatment costs, access to care, and reimbursement policies. In addition, the study will examine how myopia and its treatments affect daily activities and evaluate treatment satisfaction. No data on the efficacy of myopia treatments is collected in this study, and neither is the occurrence of adverse events.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
Inclusion Criteria: * Parents (or other proxy) of children or adolescents aged 5 years or older suffering from myopia (low, moderate, or high myopia) defined by their spherical equivalent (SER): Low myopia is from -0.5 D (inclusive) to -3.0 D (inclusive), Moderate myopia is from -3.0 D to -6.0 D (inclusive) and High myopia is \<-6.0 D. * Adults suffering from myopia and its complications such as: cataract, macular degeneration, open-angle glaucoma, retinal detachment, and legal blindness/severe visual impairment. * Patients where myopia is a known or likely contributing factor to the complication. Exclusion Criteria: * Parents (or other proxy) of children aged 4 years and below. * Patients where the complication is likely unrelated to myopia (e.g., cataract caused by diabetes) will be excluded
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| Copenhagen University Hospital | Copenhagen, Denmark | — |
| University Hospital Necker Enfants Malades | Paris, France | — |
| Klinik für Augenheilkunde (Universitätsklinikum Freiburg) | Freiburg im Breisgau, Germany | — |
| Universitäts-Augenklinik Mainz | Mainz, Germany | — |
| Meyer Children's Hospital IRCCS | Florence, Italy | — |
| Policlinico Universitario Agostino Gemelli IRCCS | Rome, Italy | — |
| Estudio Oftalmologico | Madrid, Spain | — |
| The San Carlos Clinic Hospital (Hospital Clinico San Carlos-HCSC) | Madrid, Spain | — |
| St. Erik Eye Hospital | Solna, Sweden | — |
| Moorfields Eye Hospital NHS Foundation Trust | London, United Kingdom | — |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT06912802