Real World Outcomes of Intravitreal Anti-vascular Endothelial Growth Factors for Neovascular Age Related Macular Degeneration in Taiwan
- Sponsor
- Changhua Christian Hospital
- Study ID
- NCT03324542
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Aflibercept [Eylea] — DRUGAnti-vascular endothelial growth factor (VEGF)
Study Details
Purpose To report the long-term efficacy of patients with neovascular age-related macular degeneration (nAMD) treated with anti-vascular endothelial growth factor (VEGF) in Changhua Christian Hospital in Taiwan. Method Retrospective case series of patients with nAMD that were treated with intravitreal injection of anti-VEGF and had a minimum follow up of 48 months. Every patient was initially treated with 3 loading doses of either bevacizumab or ranibizumab, followed by a loose treat and extend regimen. Eyes were divided into 2 groups according to whether aflibercept was later used as a rescue therapy (group 2) or not (group 1). Patients underwent best-corrected visual acuity (BCVA) testing, optical coherence tomography, and ophthalmic examination at baseline and all the scheduled follow-up visits.
Key Dates
- Start date
- Apr 3, 2017
- Status verified
- Jul 2018
- Primary completion
- Oct 13, 2017
- Completion
- Oct 15, 2017
Study Design
- Enrollment
- 63 participants (actual)
Primary Outcome Measure
Wilcoxon test [ Time Frame: Baseline, 12 month, 24 month, 36 month, 48 month. ]
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