Intermediate distance visual acuity in the Clareon monofocal intraocular lenses
Not Applicable
Recruiting
- Conditions
- pseudophakia
- Registration Number
- JPRN-UMIN000049822
- Lead Sponsor
- Medical Corporation Sugita Eye Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1.Patients with ocular diseases affecting visual function other than cataract 2.Patients with corneal irregular astigmatism 3.Glaucoma patients 4.Patients with a history of corneal refractive surgery, endophthalmic surgery, and keratoplasty 5.Patients deemed inappropriate by the responsible physician or subspecialist due to systemic or ophthalmologic diseases
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Binocular best corrected distance visual acuity at 3 months after surgery
- Secondary Outcome Measures
Name Time Method 1.Binocular naked eye far visual acuity at 3 months after surgery 2.Binocular far-corrected intermediate visual acuity ( 80cm, 66cm) at 3 months after surgery 3.Binocular naked eye intermediate visual acuity ( 80cm, 66cm) at 3 months after surgery 4.Best corrected far visual acuity in one eye 3 months after surgery 5.Naked eye far visual acuity of one eye at 3 months after surgery 6.Postoperative intermediate distance-corrected visual acuity of one eye at 3 months ( 80cm, 66cm) 7.Naked eye intermediate visual acuity of one eye at 3 months after surgery ( 80cm, 66cm) 8.Defocused curves 3 months after surgery 9.Postoperative refractive error 10.Distribution of visual acuity