Impact of Intravitreal Aflibercept Injections on Capillary Non-Perfusion
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Ophthalmic Consultants of Boston
- Study ID
- NCT01724554
- Phase
- PHASE1/PHASE2
- Status
- Completed
Conditions
- Central Retinal Vein Occlusion
- Proliferative Diabetic Retinopathy
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Intravitreal Aflibercept Injection — DRUGAflibercept administered to the eye intravitreally either every month or every other month.
Study Details
The purpose of this study is to look at how effective, safe, and well tolerated Intravitreal Aflibercept Injection is in subjects with Central Retinal Vein Occlusion (CRVO) or Proliferative Diabetic Retinopathy (PDR).
Key Dates
- Start date
- Nov 30, 2012
- Status verified
- May 2015
- Primary completion
- Oct 31, 2014
- Completion
- Oct 31, 2014
Study Design
- Enrollment
- 24 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Every Month TreatmentPatients will receive Intravitreal Aflibercept Injection (IAI) every month for the 12 month duration of the study.
- Experimental: Every Month, then Every Other MonthPatients will receive Intravitreal Aflibercept Injection (IAI) every month for the first 6 months, then every other month for the next 6 months. Retreatment criteria will allow for patients to be treated every month in the second 6 months if needed.
Primary Outcome Measure
Mean Change in Capillary Non-Perfusion [ Time Frame: 12 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Ophthalmic Consultants of Boston | Boston | Massachusetts | 02114 | - |
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