Efficacy of Ranibizumab in Combination With Photodynamic Therapy for Wet Age-Related Macular Degeneration
Primary Purpose
Macular Degeneration, Visual Acuity
Status
Unknown status
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Ranibizumab
Ranibizumab
Ranibizumab
Sponsored by
About this trial
This is an interventional treatment trial for Macular Degeneration focused on measuring ranibizumab, verteporfin
Eligibility Criteria
Inclusion Criteria:
- diagnosed with any subtype of primary subfoveal or juxtafoveal choroidal neovascularization
- must be 50 years of age or older
- have a lesion whose total size is no more than 5400micrometres in greatest linear dimension in the study eye
- CNV that is more than 50% obscured by blood
- have best corrected visual acuity of 20/50-20/320 (Snellen equivalent)
- have been assessed with the use of early treatment diabetic retinopathy study charts
Exclusion Criteria:
- previous treatment (including verteporfin therapy) that could compromise an assessment of the study treatment
- any permanent structural damage to the central fovea
Sites / Locations
- The Royal Victoria Hospital and the Montreal Retinal Institute
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Pre-PDT
Post-PDT
No PDT
Arm Description
Participants in this group will receive an intraocular Ranibizumab injection one week prior to the first PDT with verteporfin.
Participants in this group will receive an intraocular Ranibizumab injection one week post the first PDT with verteporfin.
Participants in this group will receive an intraocular Ranibizumab injection with no accompanying PDT with verteporfin.
Outcomes
Primary Outcome Measures
Mean change from baseline at 6 months in the best corrected visual acuity (VA) score using an early treatment diabetic retinopathy study eye chart at a starting distance of 4 meters.
Secondary Outcome Measures
To determine the following: 1:Proportion of subjects who loose fewer than 15 letters from baseline visual acuity at 6 months 2: Proportion of subjects with VA of 20/200 or worse 3: Proportion of subjects with VA of 20/40 or better
Full Information
NCT ID
NCT00813891
First Posted
December 22, 2008
Last Updated
December 22, 2008
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
1. Study Identification
Unique Protocol Identification Number
NCT00813891
Brief Title
Efficacy of Ranibizumab in Combination With Photodynamic Therapy for Wet Age-Related Macular Degeneration
Official Title
Efficacy of Ranibizumab (Lucentis) in Combination With Photodynamic Therapy for Neovascular Age-Related Macular Degeneration
Study Type
Interventional
2. Study Status
Record Verification Date
December 2008
Overall Recruitment Status
Unknown status
Study Start Date
January 2009 (undefined)
Primary Completion Date
December 2009 (Anticipated)
Study Completion Date
December 2009 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of the investigators study is to look at the visual outcomes of Ranibizumab injections in combination with photodynamic therapy for the treatment of neovascular age-related macular degeneration.
Detailed Description
The main cause of severe vision loss in patients with age-related macular degeneration (AMD) is the development of choroidal neovascularization (CNV). This debilitating form of AMD affects the macula lutea, the central part of the retina, which is responsible for high resolution visual acuity. Characteristic findings in neovascular AMD include the development of new, abnormal blood vessels in the choroid layer beneath the macula otherwise known as CNV.
Current treatment options for this condition have included include laser therapy, photodynamic therapy (PDT), and intraocular injections (different types of anti-vascular endothelial growth factors) alone or in combination. While current treatments were demonstrated to slow the progression of vision loss, neither therapy was shown to significantly improve visual acuity.
Given their different modes of action, it is believed that combination therapy of Ranibizumab with PDT may lead to better visual outcomes and may result in an improved effect in treating AMD and therefore may help decrease the need for monthly Ranibizumab injections. After the first injection, regardless of which group the patient has been assigned to, they will receive Ranibizumab injections at 4 week intervals if clinically indicated. The purpose of the this study is to evaluate the visual outcomes of intraocular Ranibizumab injections in combination with photodynamic therapy with verteporfin for the treatment of neovascular AMD.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Macular Degeneration, Visual Acuity
Keywords
ranibizumab, verteporfin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
180 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Pre-PDT
Arm Type
Active Comparator
Arm Description
Participants in this group will receive an intraocular Ranibizumab injection one week prior to the first PDT with verteporfin.
Arm Title
Post-PDT
Arm Type
Active Comparator
Arm Description
Participants in this group will receive an intraocular Ranibizumab injection one week post the first PDT with verteporfin.
Arm Title
No PDT
Arm Type
Active Comparator
Arm Description
Participants in this group will receive an intraocular Ranibizumab injection with no accompanying PDT with verteporfin.
Intervention Type
Drug
Intervention Name(s)
Ranibizumab
Other Intervention Name(s)
Lucentis the brand name of Ranibizumab
Intervention Description
Intraocular injection of 0.5mg of Ranibizumab one week prior to PDT with verteporfin
Intervention Type
Drug
Intervention Name(s)
Ranibizumab
Other Intervention Name(s)
Lucentis the brand name of Ranibizumab
Intervention Description
Intraocular injection of 0.5mg of Ranibizumab one week after PDT with verteporfin
Intervention Type
Drug
Intervention Name(s)
Ranibizumab
Other Intervention Name(s)
Lucentis the brand name of Ranibizumab
Intervention Description
Intraocular injection of 0.5mg of Ranibizumab with no accompanying PDT with verteporfin
Primary Outcome Measure Information:
Title
Mean change from baseline at 6 months in the best corrected visual acuity (VA) score using an early treatment diabetic retinopathy study eye chart at a starting distance of 4 meters.
Time Frame
Monthly for a total of 12 months
Secondary Outcome Measure Information:
Title
To determine the following: 1:Proportion of subjects who loose fewer than 15 letters from baseline visual acuity at 6 months 2: Proportion of subjects with VA of 20/200 or worse 3: Proportion of subjects with VA of 20/40 or better
Time Frame
One year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
diagnosed with any subtype of primary subfoveal or juxtafoveal choroidal neovascularization
must be 50 years of age or older
have a lesion whose total size is no more than 5400micrometres in greatest linear dimension in the study eye
CNV that is more than 50% obscured by blood
have best corrected visual acuity of 20/50-20/320 (Snellen equivalent)
have been assessed with the use of early treatment diabetic retinopathy study charts
Exclusion Criteria:
previous treatment (including verteporfin therapy) that could compromise an assessment of the study treatment
any permanent structural damage to the central fovea
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
John Galic, MD
Phone
514-285-8866
First Name & Middle Initial & Last Name or Official Title & Degree
Karin Oliver, MD
Phone
514-285-8866
Email
karin.oliver@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Galic, MD
Organizational Affiliation
Montreal Retina Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
John Chen, MD
Organizational Affiliation
Montreal Retina Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Royal Victoria Hospital and the Montreal Retinal Institute
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3Z 1P4
Country
Canada
12. IPD Sharing Statement
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Efficacy of Ranibizumab in Combination With Photodynamic Therapy for Wet Age-Related Macular Degeneration
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