Intravitreal Injection of Ranibizumab Versus Sham Before Vitrectomy in Patients With Proliferative Diabetic Retinopathy
Primary Purpose
Proliferative Diabetic Retinopathy
Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
ranibizumab
sham
pars plana vitrectomy
Sponsored by
About this trial
This is an interventional treatment trial for Proliferative Diabetic Retinopathy
Eligibility Criteria
Inclusion Criteria:
- type I or type II diabetes
- there is clear indications for vitrectomy due to proliferative membrane in the vitreoretinal interface, mild hemorrhage, or tractional retinal detachment
- retinal large vessels could be detected within one PD away from the edge of optic disc by OCT
- microcurculation could be detected by FFA in at least one quadrant
- the patient could tolerant FFA examination
Exclusion Criteria:
- a history of vitrectomy or scleral bucke in the included eye
- retinal laser photocoagulation treatment within 90 days in the included eye
- anti-VEGF treatment with 90 days in either eye
- there is cocurrent neovascular glaucoma in the included eye
- any reason that might hinde the procedure of vitrectomy, FFA OCT or the observation of ocular fudus
- a history of cere-brovascular accident or heart stroke
- renal failure
- could not attend follow up regularly
Sites / Locations
- Zhongshan Ophthalmic Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
ranibizumab
control
Arm Description
Intravitreal Injection of 0.5 mg ranibizumabone week before vitrectomy.
Sham intravitreal injection one week before vitrectomy.
Outcomes
Primary Outcome Measures
perioperative hemorrhage of the surgical eye
Secondary Outcome Measures
size of retinal non-perfusion area assessed by fluorescene angiography
macular retinal thickness assessed with optical coherance tomography
retinal vessel oxygen saturation measured with a retinal oximeter
best-corrected visual acuity
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02857491
Brief Title
Intravitreal Injection of Ranibizumab Versus Sham Before Vitrectomy in Patients With Proliferative Diabetic Retinopathy
Official Title
Comparison of Intravitreal Injection of Ranibizumab Versus Sham Injection Before Vitrectomy in Patients With Proliferative Diabetic Retinopathy: a Single-center, Prospective Double-blinded Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
July 2014 (undefined)
Primary Completion Date
September 30, 2017 (Actual)
Study Completion Date
September 30, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sun Yat-sen University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Certain percent of the eyes with proliferative diabetic retinopathymay require pars plana vitrectomy (PPV) due to vitreous haemorrhage, proliferative membrane, and tractional retinal detachment. This study will compare intravitreal injection of anti-vascular endothelial growth factor (ranibizumab) versus sham injection before vitrectomy for PDR. The main focus is to see if pre-operative injection of ranibizuman can reduce peri-operative hemorrahge related complications.
Detailed Description
Eyes responding to panretinal photocoagulation can remain stable for decades, but incomplete responses and relapses can occur in a certain percent of diabetic patients showing as proliferative diabetic retinopathy. At present vitrectomy is the main intervention for those eyes with vitreous hemorrhage, proliferative membrane, and tractional retinal detachment. And the surgical procedure might be complicated because of intraoperative bleeding. And post-operative complications might be also involved. Perioperative use of intraocular anti-VEGF might be associated with less hemorrhage related complications and better visula acuity. This study will compare intravitreal injection of anti-vascular endothelial growth factor (ranibizumab) versus sham injection one week before surgery. The investigators tried to make sure whether pre-operative injection of ranibizuman can reduce reduce intra-operative bleeding, reduce the frequency of using endodiathermy, decrease surgical time, improve microcurculation of retina, and elevte best-corrected visual acuity.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Proliferative Diabetic Retinopathy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
ranibizumab
Arm Type
Experimental
Arm Description
Intravitreal Injection of 0.5 mg ranibizumabone week before vitrectomy.
Arm Title
control
Arm Type
Sham Comparator
Arm Description
Sham intravitreal injection one week before vitrectomy.
Intervention Type
Drug
Intervention Name(s)
ranibizumab
Other Intervention Name(s)
Lucentis
Intervention Description
intravitreal injection of 0.5 mg ranibizumab before vitrectomy
Intervention Type
Drug
Intervention Name(s)
sham
Other Intervention Name(s)
control
Intervention Description
sham intravitreal injection before vitrectomy
Intervention Type
Procedure
Intervention Name(s)
pars plana vitrectomy
Other Intervention Name(s)
vitrectomy
Intervention Description
surgical procedure to remove the intravitreal hemorrhage and fibrosis membrane, and re-attach the retina, and perform endo laser photocoagulation on retina.
Primary Outcome Measure Information:
Title
perioperative hemorrhage of the surgical eye
Time Frame
3 month
Secondary Outcome Measure Information:
Title
size of retinal non-perfusion area assessed by fluorescene angiography
Time Frame
3 month
Title
macular retinal thickness assessed with optical coherance tomography
Time Frame
3 month
Title
retinal vessel oxygen saturation measured with a retinal oximeter
Time Frame
3 months
Title
best-corrected visual acuity
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
complications
Description
other perioperative complications
Time Frame
3 months
Title
surgical time
Time Frame
1 day
Title
grade of surgical difficulty
Time Frame
1 day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
type I or type II diabetes
there is clear indications for vitrectomy due to proliferative membrane in the vitreoretinal interface, mild hemorrhage, or tractional retinal detachment
retinal large vessels could be detected within one PD away from the edge of optic disc by OCT
microcurculation could be detected by FFA in at least one quadrant
the patient could tolerant FFA examination
Exclusion Criteria:
a history of vitrectomy or scleral bucke in the included eye
retinal laser photocoagulation treatment within 90 days in the included eye
anti-VEGF treatment with 90 days in either eye
there is cocurrent neovascular glaucoma in the included eye
any reason that might hinde the procedure of vitrectomy, FFA OCT or the observation of ocular fudus
a history of cere-brovascular accident or heart stroke
renal failure
could not attend follow up regularly
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lin Lu
Organizational Affiliation
Zhongshan Ophthalmic Center, Sun Yat-sen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zhongshan Ophthalmic Center
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510060
Country
China
12. IPD Sharing Statement
Plan to Share IPD
No
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Intravitreal Injection of Ranibizumab Versus Sham Before Vitrectomy in Patients With Proliferative Diabetic Retinopathy
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