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

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

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 Treatment
    Patients will receive Intravitreal Aflibercept Injection (IAI) every month for the 12 month duration of the study.
  • Experimental: Every Month, then Every Other Month
    Patients 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)

FacilityCityStateZIPSite coordinators
Ophthalmic Consultants of BostonBostonMassachusetts02114-

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