Caregiver Burden of Wet Age-related Macular Degeneration (wAMD) in Japan
- Sponsor
- Bayer
- Study ID
- NCT02541084
- Status
- Completed
Conditions
- Wet Macular Degeneration
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Aflibercept (Eylea, VEGF Trap-Eye, BAY86-5321) — DRUGAnti-VEGF therapy following the Summary of Product Characteristics
Study Details
This study aims at investigation of the caregiver burden of Wet Age-related Macular Degeneration (wAMD) patients and at the assessment of how much of caregiver burden could be reduced in transitioning from Pro Re Nata to proactive therapy especially in real-life rural settings where public transportations are not readily available.
Key Dates
- Start date
- Aug 18, 2015
- Status verified
- Aug 2017
- Primary completion
- Mar 30, 2016
- Completion
- Jul 30, 2016
Study Design
- Enrollment
- 72 participants (actual)
Arms
- Arm: PRN groupwAMD-patients treated with anti-VEGF therapy ´pro re nata´ (PRN)
- Arm: TAE groupwAMD-patients treated with anti-VEGF therapy ´treat-and-extend´ (TAE)
- Arm: PRN-to-TAE switcher groupwAMD patients treated with anti-VEGF therapy and switching from PRN to TAE regimens
Primary Outcome Measure
Degree of caregiving burden on caregivers (BIC-11) [ Time Frame: At enrollment ]
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