A study of visual function in 5-year postoperative patients with the multifocal posterior chamber lens LENTIS Comfort
Not Applicable
- Conditions
- Patients after cataract surgery
- Registration Number
- JPRN-UMIN000048353
- Lead Sponsor
- Santen Pharmaceutical Co., Ltd.
- Brief Summary
Refer to published paper
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with complications (eye or systemic) that affect postoperative visual function not related to LC implantation
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method