The interventional study of Peli lenses for functional vision improvement in patients with visual field loss
Not Applicable
- Conditions
- Visual field defect
- Registration Number
- ChiCTR2400088823
- Lead Sponsor
- Shenzhen Eye Hosiptal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- Aged between 18 and 60 years, male or female.<br>2. Corrected visual acuity in both eyes =0.8, without any visual field defects.<br>3. No chronic diseases, no history of major surgery or severe trauma. No known brain diseases such as epilepsy, brain tumors, cerebrovascular diseases, etc.<br>4. No intellectual developmental disorders, possessing normal cognitive and intellectual levels. No abnormal limb movements, normal physical motor functions.<br>5. No eye diseases that affect the visual field, such as macular degeneration, retinal detachment, optic atrophy, etc.<br>6. Voluntarily signs the informed consent form, understands the content of the study, and is willing to cooperate with the research process.
Exclusion Criteria
- Age not between 18 and 60 years.<br>2. Patients who cannot cooperate with various examinations, and whose worst corrected visual acuity is below 0.5.<br>3. Patients with intellectual developmental disorders, cognitive impairments, abnormal limb movements, or motor function disorders.<br>4. Patients with a known history of brain diseases, such as epilepsy, brain tumors, cerebrovascular diseases, etc. Those with a history of major surgery or severe trauma.<br>5. Patients deemed unsuitable for this study by the researchers.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual field;The number of collisions in the simulated environment;
- Secondary Outcome Measures
Name Time Method