Study to Assess the EffectiVeness of exIsting Anti-vascular Endothelial groWth Factor (Anti-VEGF) Treatment Regimens in Patients With Wet Age-related Macular Degeneration

Sponsor
Bayer
Study ID
NCT01933152
Status
Completed

Conditions

Eligibility Criteria

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

Interventions

  • Ranibizumab — DRUG
    Patients with wet AMD treated with ranibizumab as prescribed by physician

Study Details

Retrospective, non-interventional, observational multi-center field study. Patients diagnosed with wet Age-related macular degeneration (wAMD) and having started treatment with ranibizumab between January 1, 2009 and December 31, 2009 must be consecutively screened and, if eligible, enrolled. Patients will be followed up at maximum until December 31, 2011. Switch to any other Anti vascular endothelial growth factor (anti VEGF) treatment will be documented. For each patient, demographics, medical history, administered treatments, results of ocular and visual assessments and other tests (where available) will be documented.

Key Dates

First listed
Sep 2, 2013
Start date
Aug 31, 2012
Status verified
Sep 2014
Primary completion
Apr 30, 2013
Completion
Apr 30, 2013

Study Design

Enrollment
137 participants (actual)

Arms

  • Arm: Group 1

Primary Outcome Measure

Changes in visual acuity after start of Anti vascular endothelial growth factor (anti VEGF) therapy with ranibizumab, assessed by Early Treatment Diabetic Retinopathy (ETDRS) or Snellen chard [ Time Frame: Baseline and 24 months ]

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