Overview
To Describe the Use of Intravitreal Aflibercept and to Describe Follow-up as Well as Treatment Patterns in Patients With Wet Age-related Macular Degeneration (wAMD) or Diabetic Macular Edema (DME) in Routine Clinical Practice in Canada.
Status:
Completed
Completed
Trial end date:
2018-01-26
2018-01-26
Target enrollment:
0
0
Participant gender:
All
All
Summary
To describe the use of intravitreal aflibercept in routine clinical practice and to describe follow-up as well as treatment patterns in patients with wAMD or DME in routine clinical practice in Canada for a study population of treatment naive patients and those who have received prior therapy (anti-VEGF injections, laser, steroids, etc).Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
BayerCollaborator:
Regeneron PharmaceuticalsTreatments:
Aflibercept
Criteria
Inclusion Criteria:- Age: >= 18 years of age
- Male or female
- Patients with wet AMD (wet age-related macular degeneration) or Diabetic macular edema
(DME) who will be treated by intravitreal aflibercept according to the Canadian
Product monograph recommendations and routine clinical practice.
- Decision to treat with intravitreal aflibercept prior to patient enrolment as per the
physician's routine clinical practice.
Exclusion Criteria:
- Patients participating in an investigational program with interventions outside of
routine clinical practice.
- Patients currently being treated with intravitreal aflibercept. This study will only
include patients new to intravitreal aflibercept, both naïve and previously treated
with other anti-VEGF therapies.
- Patients who are hypersensitive to this drug, to any ingredient in the formulation, or
to any component of the container.
- Patients who are hypersensitive to this drug, to any ingredient in the formulation, or
to any component of the container.
- Ocular or peri-ocular infection
- Active intraocular inflammation
- Scar, fibrosis, or atrophy involving the center of the fovea in the study eye.
- Any concomitant therapy with another agent to treat wet AMD or DME in the study eye.