Sub-macular Injection of Ranibizumab as a New Surgical Treatment for Refractory Diabetic Macular Edema
Primary Purpose
Diabetic Macular Edema
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Sub-macular injection of Ranibizumab
Sponsored by
About this trial
This is an interventional treatment trial for Diabetic Macular Edema
Eligibility Criteria
Inclusion Criteria:
- refractory diffuse non tractional DME.
- Central retinal thickness (CRT) should exceed 350 µm despite undergoing multiple anti-VEGF therapy.
- Decimal best corrected visual acuity (BCVA) must be ≥0.01 and ≤0.5.
Exclusion Criteria:
- Previous vitrectomy, recent cataract surgery less than 6 months,
- evident RPE atrophy, proliferative diabetic retinopathy, massive foveal hard exudation, foveal traction on OCT,
- glaucoma and one eyed patients.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Persistent Diabetic macular edema
Arm Description
Authors defined refractory DME as eyes with persistent DME despite receiving at least 6 monthly Ranibizumab injections of anti VEGF, and then switched to Aflibercept, receiving at least three monthly injections.
Outcomes
Primary Outcome Measures
The primary endpoint for this study was the change in CMT at the final visit.
Central macular thickness
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03975088
Brief Title
Sub-macular Injection of Ranibizumab as a New Surgical Treatment for Refractory Diabetic Macular Edema
Official Title
Sub-macular Injection of Ranibizumab as a New Surgical Treatment for Refractory Diabetic Macular Edema
Study Type
Interventional
2. Study Status
Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
January 1, 2017 (Actual)
Primary Completion Date
December 31, 2017 (Actual)
Study Completion Date
December 31, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alexandria
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The best treatment strategy for refractory DME is not known, options include switching between anti-VEGF agents, corticosteroids, and vitrectomy. In this study, authors describe a new surgical technique for the treatment of refractory non tractional DME. The technique consists of vitrectomy with ILM peeling with subretinal injection of Ranibizumab.
Detailed Description
Purpose: In this study, authors describe a new surgical technique for the treatment of refractory DME. The technique consists of vitrectomy with ILM peeling with subretinal injection of Ranibizumab.
Methods: This is a prospective interventional non-comparative study including patients with refractory DME. Included patients were subjected to the new surgical technique of pars plana vitrectomy with sub-retinal injection of Ranibizumab.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Macular Edema
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
19 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Persistent Diabetic macular edema
Arm Type
Other
Arm Description
Authors defined refractory DME as eyes with persistent DME despite receiving at least 6 monthly Ranibizumab injections of anti VEGF, and then switched to Aflibercept, receiving at least three monthly injections.
Intervention Type
Procedure
Intervention Name(s)
Sub-macular injection of Ranibizumab
Intervention Description
In this study, authors describe a new surgical technique for the treatment of refractory non tractional DME. The technique consists of vitrectomy with ILM peeling with subretinal injection of Ranibizumab.
Primary Outcome Measure Information:
Title
The primary endpoint for this study was the change in CMT at the final visit.
Description
Central macular thickness
Time Frame
at the 6 month follow up visit
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
refractory diffuse non tractional DME.
Central retinal thickness (CRT) should exceed 350 µm despite undergoing multiple anti-VEGF therapy.
Decimal best corrected visual acuity (BCVA) must be ≥0.01 and ≤0.5.
Exclusion Criteria:
Previous vitrectomy, recent cataract surgery less than 6 months,
evident RPE atrophy, proliferative diabetic retinopathy, massive foveal hard exudation, foveal traction on OCT,
glaucoma and one eyed patients.
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
proecting patient privacy
Citations:
PubMed Identifier
31772766
Citation
El-Baha SM, Abdel Hadi AM, Abouhussein MA. Submacular Injection of Ranibizumab as a New Surgical Treatment for Refractory Diabetic Macular Edema. J Ophthalmol. 2019 Oct 21;2019:6274209. doi: 10.1155/2019/6274209. eCollection 2019.
Results Reference
derived
Learn more about this trial
Sub-macular Injection of Ranibizumab as a New Surgical Treatment for Refractory Diabetic Macular Edema
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