Study of the efficacy and safety of intra-retinal arterial fibrinolysis for central retinal artery occlusio
Not Applicable
Recruiting
- Conditions
- Central Retinal Artery Occlusion(CRAO)
- Registration Number
- JPRN-UMIN000022972
- Lead Sponsor
- Yokohama City University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients who may have side effects by tPA 2)Pregnancy 3)Patients judged to be appropriate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual acuity 24 weeks after surgery
- Secondary Outcome Measures
Name Time Method 1) Improvement of visual acuity from baseline to 24 weeks after surgery 2) Change of retinal thickness from baseline to 24 weeks after surgery 3) Laser speckle from baseline to 24 weeks after surgery 4) Occurrence rate of surgical complications 5) Vison loss