Avastin for PDR (Proliferative Diabetic Retinopathy) (PDR)
Primary Purpose
Retinal Detachment, Diabetic Retinopathy
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Avastin (bevacizumab)
Sham injection
Sponsored by
About this trial
This is an interventional treatment trial for Retinal Detachment focused on measuring Traction Retinal Detachment (PDR), Proliferative Diabetic Retinopathy (PDR)
Eligibility Criteria
Inclusion Criteria:
- Active fibrovascular proliferation due to PDR with TRD given pre-operative clearance for pars plana vitrectomy (PPV) and TRD repair.
Exclusion Criteria:
- Dense vitreous hemorrhage
- Inability to follow-up for surgery within 3-7 days after intravitreal injection
- History of stroke, thromboembolic event, or heart attack within the last 6 months
- Less than 18 years of age
- Pregnancy
Sites / Locations
- University of Southern California
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Avastin Injection Group (AIG)
Sham Injection Group (SIG)
Arm Description
Subjects in this group will get single 0.05 mL intravitreal injection of bevacizumab 1.25 mg 3-7 days prior to surgery for tractional retinal detachment secondary to Proliferative Diabetic Retinopathy.
Subjects in this group will get a sham injection 3-7 days prior to surgery for tractional retinal detachment secondary to Proliferative Diabetic Retinopathy.
Outcomes
Primary Outcome Measures
The Effect of an Anti-VEGF (Vascular Endothelial Growth Factor) Agent, Bevacizumab, on Levels of Vitreous and Aqueous Growth Factor Levels (pg/mL) in Eyes With Traction Retinal Detachment Due to PDR
Comparison of vitreous VEGF levels (pg/mL) and aqueous VEGF (pg/mL) levels in bevacizumab and control groups.
Secondary Outcome Measures
Whether Intra- and Post-operative Complications Are Decreased in Eyes Given Pre-operative Adjunctive Bevacizumab in Eyes Undergoing Proliferative Form of Diabetic Retinopathy (PDR) Surgery.
Improvement of Visual Outcomes in Patients Given Pre-operative Adjunctive Bevacizumab in Eyes Undergoing PDR Surgery.
Measured by median logMAR change in the best corrected visual acuity (VA) from baseline to post operative month 3 (POM3)
Full Information
NCT ID
NCT01270542
First Posted
December 1, 2010
Last Updated
July 14, 2017
Sponsor
University of Southern California
1. Study Identification
Unique Protocol Identification Number
NCT01270542
Brief Title
Avastin for PDR (Proliferative Diabetic Retinopathy)
Acronym
PDR
Official Title
Effect of Pre-operative Adjunctive Anti-VEGF on Growth Factors in Severe Proliferative Diabetic Retinopathy Requiring Surgical Management
Study Type
Interventional
2. Study Status
Record Verification Date
May 2014
Overall Recruitment Status
Completed
Study Start Date
June 2009 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Southern California
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine the effect of anti-VEGF drug (Avastin) adminstration in eyes prior to surgical treatment for Traction retinal detachment (TRD) in patients with Proliferative Diabetic Retinopathy (PDR).
Detailed Description
Traction retinal detachment (TRD) due to proliferative diabetic retinopathy is a blinding disease caused by contraction of fibrovascular proliferation, treatment of which is limited to surgery. Fibrosis and neovascularization are both associated with high levels of connective tissue growth factor (CTGF) and vascular endothelial growth factor (VEGF) in the eye. Small, nonrandomized studies have suggested that pre-operative adjunctive anti-VEGF administration may reduce intra- and post-operative complications and provide visual benefit in patients with this condition.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Retinal Detachment, Diabetic Retinopathy
Keywords
Traction Retinal Detachment (PDR), Proliferative Diabetic Retinopathy (PDR)
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Avastin Injection Group (AIG)
Arm Type
Experimental
Arm Description
Subjects in this group will get single 0.05 mL intravitreal injection of bevacizumab 1.25 mg 3-7 days prior to surgery for tractional retinal detachment secondary to Proliferative Diabetic Retinopathy.
Arm Title
Sham Injection Group (SIG)
Arm Type
Sham Comparator
Arm Description
Subjects in this group will get a sham injection 3-7 days prior to surgery for tractional retinal detachment secondary to Proliferative Diabetic Retinopathy.
Intervention Type
Drug
Intervention Name(s)
Avastin (bevacizumab)
Other Intervention Name(s)
Avastin
Intervention Description
single 0.05 mL intravitreal injection of bevacizumab 1.25 mg
Intervention Type
Other
Intervention Name(s)
Sham injection
Other Intervention Name(s)
Sham
Intervention Description
Subject's eyes will be anesthetized but no injection will be performed.
Primary Outcome Measure Information:
Title
The Effect of an Anti-VEGF (Vascular Endothelial Growth Factor) Agent, Bevacizumab, on Levels of Vitreous and Aqueous Growth Factor Levels (pg/mL) in Eyes With Traction Retinal Detachment Due to PDR
Description
Comparison of vitreous VEGF levels (pg/mL) and aqueous VEGF (pg/mL) levels in bevacizumab and control groups.
Time Frame
3 months after last surgery
Secondary Outcome Measure Information:
Title
Whether Intra- and Post-operative Complications Are Decreased in Eyes Given Pre-operative Adjunctive Bevacizumab in Eyes Undergoing Proliferative Form of Diabetic Retinopathy (PDR) Surgery.
Time Frame
3 months after last surgery.
Title
Improvement of Visual Outcomes in Patients Given Pre-operative Adjunctive Bevacizumab in Eyes Undergoing PDR Surgery.
Description
Measured by median logMAR change in the best corrected visual acuity (VA) from baseline to post operative month 3 (POM3)
Time Frame
3 months from last surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Active fibrovascular proliferation due to PDR with TRD given pre-operative clearance for pars plana vitrectomy (PPV) and TRD repair.
Exclusion Criteria:
Dense vitreous hemorrhage
Inability to follow-up for surgery within 3-7 days after intravitreal injection
History of stroke, thromboembolic event, or heart attack within the last 6 months
Less than 18 years of age
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dean Eliott, MD
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Southern California
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
22965588
Citation
Sohn EH, He S, Kim LA, Salehi-Had H, Javaheri M, Spee C, Dustin L, Hinton DR, Eliott D. Angiofibrotic response to vascular endothelial growth factor inhibition in diabetic retinal detachment: report no. 1. Arch Ophthalmol. 2012 Sep;130(9):1127-34. doi: 10.1001/archophthalmol.2012.1611.
Results Reference
derived
Learn more about this trial
Avastin for PDR (Proliferative Diabetic Retinopathy)
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