Development and clinical application of an optical mouse detection device for the treatment of amblyopia caused by congenital nystagmus, sway vision in acquired nystagmus, and reduction of diplopia in acquired strabismus
Not Applicable
Recruiting
- Conditions
- Congenital nystagmus, acquired nystagmus, strabismus
- Registration Number
- JPRN-UMIN000046924
- Lead Sponsor
- Kitasato University School of Allied Health Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
Exclusion Criteria for Stage 1 Previous external eye surgery for strabismus or nystagmus Pregnant women who are at least 5 months old before the examination Exclusion criteria for stage 2 Previous or planned external eye surgery for strabismus or nystagmus Patients with corneal or retinal diseases other than nystagmus that cause poor vision. Patients with functional amblyopia, etc., who are expected to improve their visual function with visual function training within the scope of regular medical care.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method An optical mouse detection system (self-made optical device) will be loaned to the participants, and they will be trained to wear it for 3 hours a day at home. Training will be conducted for 30 days, and the patient will be asked to visit the ophthalmology outpatient clinic after 30 days. After that, the training and ophthalmology outpatient visits will be repeated, and a 6-month study will be conducted to evaluate the visual function.
- Secondary Outcome Measures
Name Time Method