Maximum Treatment Interval With Aflibercept T&E
- Sponsor
- Shin Kong Wu Ho-Su Memorial Hospital
- Study ID
- NCT05342857
- Status
- Unknown
Conditions
- Neovascular Age-related Macular Degeneration
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Aflibercept Injection [Eylea] — DRUGAflibercept 2.0 mg with the T\&E criteria in Taiwan local consensus
Study Details
To evaluate the duration of effectiveness of anti-VEGF (Aflibercept) by analyzing the percentage of patients whose maximum treatment interval is extended to 16 weeks and beyond in 24 months and their long-term remission.
Key Dates
- Start date
- Jan 1, 2022
- Status verified
- Apr 2022
- Primary completion
- Aug 31, 2024
- Completion
- Apr 30, 2025
Study Design
- Enrollment
- 100 participants (estimated)
Primary Outcome Measure
The percentage of patients whose maximum treatment interval is extended to 24 months [ Time Frame: 2 years ]
Central Contacts
- Cheng-Kuo Cheng, MD886-2833-2211
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