Clinical trials of FineVision (PhysIOL) trifocal intraocular lens
Not Applicable
- Conditions
- Cataract causing impaired visual function
- Registration Number
- JPRN-UMIN000024869
- Lead Sponsor
- Kanazawa Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 33
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with a history of ocular diseases including: age-related macular degeneration of the macula; advanced glaucoma (severe visual field abnormality); keratoconus; ruptured Zinn's zonule and other corneal diseases. Patients with a history of cornea refractive surgery and patients excluded by a responsible doctor for other reasons to be stated.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual acuity (VA; non-corrected VA, corrected VA, contrast VA, functional VA, near distance VA, etc.)is measured the next day after surgery, one week, one month, three months, six months, one year, then every year.
- Secondary Outcome Measures
Name Time Method refraction, accommodative power, form of anterior ocular segment, corneal endothelium, corneal form, corneal thickness, pupil diameter, forward light scattering, backward light scattering, higher-order aberrations, retinal image contrast, diagnosis of anterior ocular segment by slit-lamp microscopy, measurement of anterior chamber protein content