Prospective Comparative Study between Digitally Assisted Vitreoretinal Surgery and Analog Microscope Systems Regarding Color Contrast and Surgical Ergonomics
Not Applicable
Recruiting
- Conditions
- Diseases of the eye and adnexa
- Registration Number
- KCT0006210
- Lead Sponsor
- Kyungpook National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Patients with ERM or macular hole requiring ILM peeling
- Ability to be able to meet follow-up requirements
- A person who voluntarily decides to participate in clinical trial and signs a consent form
Exclusion Criteria
- A history of previous vitrectomy
- Patients with any other retinal or choroidal diseases including diabetic retinopathy, retinal vein occlusion, retinal detachment, uveitis, and age-related macular degeneration
- A history of ocular trauma including corneoscleral laceration
- Corneal diseases including corneal opacity or corneal dystrophy
- Follow-up period less than 3 months during clinical trial
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of the mean color contrast ratio of groups receiving different concentrations (range: 0.075% to 0.0125%) of ICG dye.
- Secondary Outcome Measures
Name Time Method Comparison of muscle tone and stiffness;Best-corrected visual acuity (BCVA);operating time