Trials / Recruiting
RecruitingNCT06912802
Observational Survey Study on the Impact of Myopia and Its Complications on Quality of Life.
Non-interventional Study to Assess the Impact of Myopia in Childhood and the Long-Term Complications in Adulthood on Health-Related Quality of Life (HRQoL).
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 350 (estimated)
- Sponsor
- Santen SAS · Industry
- Sex
- All
- Age
- 5 Years
- Healthy volunteers
- Not accepted
Summary
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Non-Intervention | Non-Intervention study |
Timeline
- Start date
- 2025-07-29
- Primary completion
- 2025-12-01
- Completion
- 2025-12-01
- First posted
- 2025-04-06
- Last updated
- 2025-08-07
Locations
10 sites across 7 countries: Denmark, France, Germany, Italy, Spain, Sweden, United Kingdom
Source: ClinicalTrials.gov record NCT06912802. Inclusion in this directory is not an endorsement.