Bevacizumab as Adjunctive Treatment to Laser Panretinal Photocoagulation for Proliferative Diabetic Retinopathy
Primary Purpose
Proliferative Diabetic Retinopathy
Status
Unknown status
Phase
Phase 2
Locations
Brazil
Study Type
Interventional
Intervention
Panretinal photocoagulation
Procedure: Panretinal Photocoagulation (PRP) Drug: Intravitreous injection of Bevacizumab
Sponsored by
About this trial
This is an interventional treatment trial for Proliferative Diabetic Retinopathy focused on measuring Proliferative Diabetic Retinopathy, Bevacizumab, Panretinal Photocoagulation
Eligibility Criteria
Inclusion Criteria:
- Proliferative diabetic retinopathy eyes.
- Best Corrected-Visual Acuity at baseline > 20/320 in the study eye.
- Patients with and without diabetic macular edema
- Type II diabetic subjects as defined by the World Health Organization
- aged ≥ 18 years.
- Women must be using effective contraception
- Ability to provide written informed consent.
- Indication of panretinal photocoagulation in both eyes
Exclusion Criteria:
- Vitreous hemorrhage or pre-retinal hemorrhage
- Eyes with prior scatter (panretinal) or focal/grid photocoagulation, within the previous 6 months.
- Atrophy/scarring/fibrosis/ hard exudates involving the center of the macula.
- Cataract
- Any intraocular surgery within 6 months before trial enrollment.
- Previous vitrectomy.
Any of the following underlying systemic diseases:
History or evidence of severe cardiac disease or previous thrombus-embolic event
Sites / Locations
- University of Sao PauloRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Panretinal photocoagulation
Bevacizumab + Panretinal Photocoagulation (PRP)
Arm Description
Group 1: Panretinal photocoagulation treatment (PRP) at month-0 that can be repeated after month-3.
Group 2: Bevacizumab intravitreous injections plus PRP
Outcomes
Primary Outcome Measures
Functional Macular Evaluation
During this 24 weeks of follow-up the Visual acuity (ETDRS), Contrast vision will be measured at baseline, 4, 12 and finally at 24 week
Secondary Outcome Measures
Structural Macular Evaluation
During the 24 weeks of follow-up the following measured will be made: Optical coherence tomography, need of vitrectomy, need panretianal photocoagulation retreatment, adverse events, recurrence of neovascularizaton, need or additional focal and grid macular laser for diabetic macular edema
Full Information
NCT ID
NCT01389505
First Posted
July 5, 2011
Last Updated
July 7, 2011
Sponsor
Instituto do Coracao
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
1. Study Identification
Unique Protocol Identification Number
NCT01389505
Brief Title
Bevacizumab as Adjunctive Treatment to Laser Panretinal Photocoagulation for Proliferative Diabetic Retinopathy
Official Title
Structural and Functional Evaluation of the Macula in Patients With Proliferative Diabetic Retinopathy Treated With Panretinal Photocoagulation and Bevacizumab (Avastin ®)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2011
Overall Recruitment Status
Unknown status
Study Start Date
February 2011 (undefined)
Primary Completion Date
September 2012 (Anticipated)
Study Completion Date
September 2012 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Instituto do Coracao
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a prospective, randomized and comparative study is to quantify the functional and structural alterations of the macula in patients with proliferative Diabetic Retinopathy submitted to laser photocoagulation and to evaluate the efficacy of intravitreal bevacizumab as a adjuvant therapy in preventing the adverse events of that procedure. The patients with proliferative Diabetic Retinopathy (DR) with indication of binocular laser photocoagulation will be examined by ophthalmologists who will measure the visual acuity and contrast sensitivity, perform slit lamp examination, fundus examination and optic coherence tomography before and after laser photocoagulation. Laser photocoagulation will be performed in both eyes according Early Treatment Diabetic Retinopathy Study that advocate the realization of 3 episodes of laser photocoagulation in 3 weeks. This comparative study analyses the effect of intravitreal bevacizumab one week before laser photocoagulation and one, three and six months after the randomization visit. The fellow eye will be submitted only to laser photocoagulation and will be considered as control. It is estimated a sample of 30 patients. All procedures, purposes and methods will be explained to all patients.
Detailed Description
The current gold standard for the treatment of proliferative diabetic retinopathy is panretinal photocoagulation. Therefore this study is designed using both treatments in the same patient: intravitreal Bevacizumab plus panretinal photocoagulation in one eye, compared to panretinal photocoagulation alone in the contralateral eye. These patients had their visual acuity and contrast vision measured and complete ophthalmological examination was performed, including macular slit lamp examination, fluorescein angiography and optical coherence tomography.
Patients with similar proliferative diabetic retinopathy without high risk characteristics receive laser therapy in both eyes and intravitreal Bevacizumab injections in one eye. For the Bevacizumab injections, numbing drops, antibiotic drops, and drops to dilate the pupil, and possibly and anesthetic injection, are put in the eye before the medicine is injected into the vitreous. Patients return for follow-up visits 1 day, 1 and 4 weeks after the injection, and then 3 and 6 months. Patients whose condition does not improve may undergo new evaluation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Proliferative Diabetic Retinopathy
Keywords
Proliferative Diabetic Retinopathy, Bevacizumab, Panretinal Photocoagulation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Panretinal photocoagulation
Arm Type
Active Comparator
Arm Description
Group 1: Panretinal photocoagulation treatment (PRP) at month-0 that can be repeated after month-3.
Arm Title
Bevacizumab + Panretinal Photocoagulation (PRP)
Arm Type
Experimental
Arm Description
Group 2: Bevacizumab intravitreous injections plus PRP
Intervention Type
Procedure
Intervention Name(s)
Panretinal photocoagulation
Intervention Description
Three episodes of panretinal photocoagulation with one week of interval
Intervention Type
Procedure
Intervention Name(s)
Procedure: Panretinal Photocoagulation (PRP) Drug: Intravitreous injection of Bevacizumab
Intervention Description
Intravitreous injection of Bevacizumab 1 week before and the other at the same day of the third episode of PRP
Primary Outcome Measure Information:
Title
Functional Macular Evaluation
Description
During this 24 weeks of follow-up the Visual acuity (ETDRS), Contrast vision will be measured at baseline, 4, 12 and finally at 24 week
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Structural Macular Evaluation
Description
During the 24 weeks of follow-up the following measured will be made: Optical coherence tomography, need of vitrectomy, need panretianal photocoagulation retreatment, adverse events, recurrence of neovascularizaton, need or additional focal and grid macular laser for diabetic macular edema
Time Frame
24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Proliferative diabetic retinopathy eyes.
Best Corrected-Visual Acuity at baseline > 20/320 in the study eye.
Patients with and without diabetic macular edema
Type II diabetic subjects as defined by the World Health Organization
aged ≥ 18 years.
Women must be using effective contraception
Ability to provide written informed consent.
Indication of panretinal photocoagulation in both eyes
Exclusion Criteria:
Vitreous hemorrhage or pre-retinal hemorrhage
Eyes with prior scatter (panretinal) or focal/grid photocoagulation, within the previous 6 months.
Atrophy/scarring/fibrosis/ hard exudates involving the center of the macula.
Cataract
Any intraocular surgery within 6 months before trial enrollment.
Previous vitrectomy.
Any of the following underlying systemic diseases:
History or evidence of severe cardiac disease or previous thrombus-embolic event
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rony C Preti, MD
Phone
+551199991636
Email
rypreti@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
University Sao Paulo
Phone
+551130696000
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Walter Y Takahashi, PhD
Organizational Affiliation
University of Sao Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Sao Paulo
City
Sao Paulo
State/Province
SP
ZIP/Postal Code
05403-000
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rony C Preti, MD
Phone
+551199991636
Email
rypreti@hotmail.com
First Name & Middle Initial & Last Name & Degree
Rony C Preti, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
28273240
Citation
Preti RC, Mutti A, Ferraz DA, Zacharias LC, Nakashima Y, Takahashi WY, Monteiro ML. The effect of laser pan-retinal photocoagulation with or without intravitreal bevacizumab injections on the OCT-measured macular choroidal thickness of eyes with proliferative diabetic retinopathy. Clinics (Sao Paulo). 2017 Feb 1;72(2):81-86. doi: 10.6061/clinics/2017(02)03.
Results Reference
derived
PubMed Identifier
23686001
Citation
Preti RC, Ramirez LM, Monteiro ML, Carra MK, Pelayes DE, Takahashi WY. Contrast sensitivity evaluation in high risk proliferative diabetic retinopathy treated with panretinal photocoagulation associated or not with intravitreal bevacizumab injections: a randomised clinical trial. Br J Ophthalmol. 2013 Jul;97(7):885-9. doi: 10.1136/bjophthalmol-2012-302675. Epub 2013 May 17.
Results Reference
derived
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Bevacizumab as Adjunctive Treatment to Laser Panretinal Photocoagulation for Proliferative Diabetic Retinopathy
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