Bevacizumab as Adjunctive Treatment to Laser Panretinal Photocoagulation for Proliferative Diabetic Retinopathy
NCT ID: NCT01389505
Last Updated: 2011-07-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE2
30 participants
INTERVENTIONAL
2011-02-28
2012-09-30
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Panretinal photocoagulation
Group 1: Panretinal photocoagulation treatment (PRP) at month-0 that can be repeated after month-3.
Panretinal photocoagulation
Three episodes of panretinal photocoagulation with one week of interval
Bevacizumab + Panretinal Photocoagulation (PRP)
Group 2: Bevacizumab intravitreous injections plus PRP
Procedure: Panretinal Photocoagulation (PRP) Drug: Intravitreous injection of Bevacizumab
Intravitreous injection of Bevacizumab 1 week before and the other at the same day of the third episode of PRP
Interventions
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Panretinal photocoagulation
Three episodes of panretinal photocoagulation with one week of interval
Procedure: Panretinal Photocoagulation (PRP) Drug: Intravitreous injection of Bevacizumab
Intravitreous injection of Bevacizumab 1 week before and the other at the same day of the third episode of PRP
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
ALL
No
Sponsors
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
OTHER_GOV
Instituto do Coracao
OTHER_GOV
Responsible Party
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Faculdade de Medicina da Universidade de Sao Paulo
Principal Investigators
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Walter Y Takahashi, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Sao Paulo
Locations
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University of Sao Paulo
São Paulo, São Paulo, Brazil
Countries
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Central Contacts
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University Sao Paulo
Role: CONTACT
Facility Contacts
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References
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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.
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.
Other Identifiers
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CONEP16249
Identifier Type: OTHER
Identifier Source: secondary_id
CONEP16249
Identifier Type: -
Identifier Source: org_study_id
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