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Comparative Study on Clinical Outcomes after Two type of Intraocular Lenses implantation with Different Diopter Interval (0.25 Diopter vs. 0.50 Diopter)

Not Applicable
Completed
Conditions
Diseases of the eye and adnexa
Registration Number
KCT0002192
Lead Sponsor
Korea University Ansan Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
40
Inclusion Criteria

Patients with expected best-corrected visual acuities (BCVA) more than 20/40 after cataract surgery
- Patients who underwent preoperative measurements of the IL Master®.
- Patients with calculated intraocular lens power range of from 15.0 to 25.0 D
- Patients with no opacity of ocular media except cataract

Exclusion Criteria

- Patients with other diseases that can affect visual acuity
- Patients with stravismus or amblyopia
- Patients who have ocular abnomliaty which can affect postoperative intraocular lens position
- Patients with corneal disease such as keratoconus or cornela dystrophy
- Patients who have histry of previous refractive surgery or ocular trauma
- Patients who are using systemic medicine or eye drops which can affect visual acuity
- Patients who are currently participating in other clinical studies or have participated in other clinical studies within 30 days of the study

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Refractive prediction error
Secondary Outcome Measures
NameTimeMethod
Corrected visual acuity
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