Long-term Results After Intravitreal Bevacizumab Treatment Of Neovascular Age-related Macular Degeneration
Primary Purpose
Neovascular Age-related Macular Degeneration
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Bevacizumab
Sponsored by
About this trial
This is an interventional treatment trial for Neovascular Age-related Macular Degeneration focused on measuring bevacizumab, choroidal neovascularization
Eligibility Criteria
Inclusion Criteria:
- any subtype of neovascular age-related macular degeneration
- age of 50 years or older
- initial treatment with intravitreal bevacizumab between August 2005 and June 2006
Exclusion Criteria:
- previous vitrectomy
- presence of cystoid macular edema without choroidal neovascularization
- Uncontrolled systemic disease
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
group 1
Arm Description
bevacizumab intravitreal injection
Outcomes
Primary Outcome Measures
Vision
Best-corrected visual acuity converted to logMAR (MAR=minimum angle of resolution) for statistical analysis
CRT (Central Retinal Thickness)
Central retinal thickness measured in µm
Secondary Outcome Measures
Systemic Complications After Treatment
Full Information
NCT ID
NCT01027468
First Posted
December 7, 2009
Last Updated
April 3, 2019
Sponsor
Medical University of Vienna
1. Study Identification
Unique Protocol Identification Number
NCT01027468
Brief Title
Long-term Results After Intravitreal Bevacizumab Treatment Of Neovascular Age-related Macular Degeneration
Official Title
Functional, Morphological And Safety Results After Intravitreal Bevacizumab Treatment Of Neovascular Age-related Macular Degeneration - 3 Years Of Follow-up
Study Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
August 2009 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
December 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Vienna
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
200 eyes with each subtype of neovascular age-related macular degeneration will be included in this study and 3 years after the initial intravitreal bevacizumab, best-corrected visual acuity (BCVA) will be measured using Snellen charts at 6m. Central retinal thickness (CRT) will be measured using Stratus OCT and Cirrus SD-OCT (Zeiss). Data of treatment-naive eyes (group 1) were compared to the data of eyes that had undergone prior treatment with photodynamic therapy with verteporfin and intravitreal triamcinolone acetonide (group 2).
Detailed Description
In this interventional clinical study, 181 eyes of 160 consecutive patients with active neovascular related macular degeneration meeting recommended criteria for inclusion and protocol criteria for anti-vascular endothelial growth factor therapy undergoing intravitreal bevacizumab monotherapy were evaluated. Data of treatment-naive eyes (Group 1, n = 114) were analyzed separately from eyes that had undergone previous photodynamic therapy plus intravitreal triamcinolone (Group 2, n = 67). Re-treatment criteria were based on clinical outcome following the official European label regimen. After 1 year of continuous service at an academic referral center, follow-up was performed in private practices in collaboration with the referral center. Main outcome parameters were best-corrected visual acuity and central retinal thickness.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neovascular Age-related Macular Degeneration
Keywords
bevacizumab, choroidal neovascularization
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
160 (Actual)
8. Arms, Groups, and Interventions
Arm Title
group 1
Arm Type
Experimental
Arm Description
bevacizumab intravitreal injection
Intervention Type
Drug
Intervention Name(s)
Bevacizumab
Other Intervention Name(s)
intraocular injection
Intervention Description
intraocular bevacizumab injection
Primary Outcome Measure Information:
Title
Vision
Description
Best-corrected visual acuity converted to logMAR (MAR=minimum angle of resolution) for statistical analysis
Time Frame
3 years after first intravitreal bevacizumab treatment
Title
CRT (Central Retinal Thickness)
Description
Central retinal thickness measured in µm
Time Frame
3 years after initial intravitreal bevacizumab treatment
Secondary Outcome Measure Information:
Title
Systemic Complications After Treatment
Time Frame
3 years after initial bevacizumab treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
any subtype of neovascular age-related macular degeneration
age of 50 years or older
initial treatment with intravitreal bevacizumab between August 2005 and June 2006
Exclusion Criteria:
previous vitrectomy
presence of cystoid macular edema without choroidal neovascularization
Uncontrolled systemic disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stefan Sacu, PD Dr.
Organizational Affiliation
Department of Ophthalmology, Medical University of Vienna, Austria
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Long-term Results After Intravitreal Bevacizumab Treatment Of Neovascular Age-related Macular Degeneration
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