The study for the effect of intravitreous injection of ranibizumab (product name: Lucentis) and subthreshold laser photocoagulation on diabetic macular edema
Phase 3
- Conditions
- diabetic macular edema
- Registration Number
- JPRN-UMIN000017037
- Lead Sponsor
- Jichi Medica University, Saitama Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who receive occular surgical treatments within 3 months Patients who receive other macular diseases
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method best-corrected visual acuity (before treatment, 3 months later, 6 months later, 12 months later) total number of injections (for 12 months) change in central retinal subfield thickness (3 months later, 6 months later, 12 months later)
- Secondary Outcome Measures
Name Time Method fluorescein angiography (before treatment, 3 months later, 6 months later, 12 months later)
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie ranibizumab's anti-VEGF effects in diabetic macular edema?
How does subthreshold laser photocoagulation synergize with ranibizumab in treating diabetic macular edema?
What biomarkers predict response to combination therapy of ranibizumab and subthreshold laser in DME patients?
What are the comparative safety profiles of ranibizumab-laser combination versus standard anti-VEGF monotherapy for DME?
How does ranibizumab combination therapy compare to aflibercept or bevacizumab in phase III DME trials?