Exploration of visual function evaluation methods and clinical endpoints in patients with ultra-low visio
- Conditions
- Inherited Retinal Disease: IRD
- Registration Number
- JPRN-UMIN000047757
- Lead Sponsor
- Keio University school of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 65
Not provided
1. Healthy people with other eye complications that significantly affect visual field or visual acuity, and with abnormal findings detected by slit-lamp microscopy, fundoscopy, OCT. 2. Those who underwent eye surgery within 3 months. 3. Subjects who have with a history of allergy to the agents to be used in this study, e.g. mydriatic agent, anesthetic agent, etc. 4. Subjects who are diagnosed with dementia or mental illness. 5. Those who are pregnant or lactating. 6. Those who are currently participating in other clinical trials. 7. Those who have participated in a clinical trial for therapeutic purposes within the past 3 months. 8. Those who with a history or suspected or confirmed diagnosis of alcohol or other drug addictions. 9. Those who unable to understand the evaluation and examination procedures. 10. Those who, in the judgment of the principal investigator, are considered to be at risk of becoming ineligible for the study. 11. Those who are judged by the principal investigator or other investigators to be inappropriate for participation in this study.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method