Myopic Maculopathy
Conditions
Interventions
Experiment Group(posterior scleral contraction group):None
Control Group(Non-posterior scleral contraction group):None
Sponsors
Eye Hospital, Wenzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: This study included high myopia patients who attended the High Myopia Clinic of our hospital from January 2012 through December 2016. 1. Age>=18 years at follow-up, male or female; 2. Axial length >=26 mm or spherical equivalent refractive error >=-6.0 diopters; 3. Complete examination records at our hospital at the time of enrollment; 4. Able to cooperate with study examinations and procedures; 5. No history of ocular trauma or trauma-related surgery; 6. Able to understand the purpose of the study, voluntarily participate, and provide signed informed consent by the patient or legal guardian.
Exclusion criteria
Exclusion criteria: 1. History of ocular trauma or trauma-related ocular surgery; 2. Presence of other vision-impairing ocular diseases (e.g., glaucoma, diabetic retinopathy, corneal opacity); 3. Incomplete medical records or examination data; 4. Inability to cooperate with study examinations due to mental disorders or other reasons; 5. Pregnant or breastfeeding women; 6. Long-term use of ocular or systemic medications that may affect visual outcomes; 7. Any other condition that, in the judgment of the investigator, would make the participant unsuitable for the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The rate of myopic maculopathy progression; | — |
Secondary
| Measure | Time frame |
|---|---|
| Axial Length;Foveal thickness;Best-Corrected Visual Acuity (BCVA);Intraocular pressure; | — |
Countries
China
Contacts
Public ContactHuifang Ye
Eye Hospital, Wenzhou Medical University
Outcome results
None listed