Clinical study of posterior chamber lens KI-362-YP in patients with senile cataract
Phase 3
- Conditions
- Senile cataract
- Registration Number
- JPRN-jRCT2080225356
- Lead Sponsor
- Kowa Company, Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- preinitiation
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Senile (age-related) cataract patients for which ultrasonic emulsification suction is indicated
etc.
Exclusion Criteria
- Patients with a disease in which the symptoms worsen during and/or after surgery in the target eye
- Patients who are participating in or will participate in other clinical trials that may affect the evaluation of this clinical trial
- Patients who are judged to be inappropriate by the principal investigator or the sub-investigator
etc.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method