New Concepts in Diabetic Macular Edema (DME) (DME)
Primary Purpose
Diabetes Mellitus, With Complications
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
INTRAVITREAL RANIBIZUMAB INJECTION
Sponsored by
About this trial
This is an interventional treatment trial for Diabetes Mellitus, With Complications focused on measuring macula-injection- laser- ranibizumab-edema-thickness
Eligibility Criteria
Inclusion Criteria:
- focal maculopathy
- diffuse macular edema
- diffuse macular edema with ischemic changes
Exclusion Criteria:
- ischemic maculopathy that was associated with grades of non-proliferative changes, or capillary drop out zones presented in the periphery of the macula
- patients with history of stroke or transient ischemic attack
- hypersensitivity to ranibizumab or any component of the ranibizumab formulation
- uncontrolled glaucoma in either eye (intraocular pressure [IOP] >24 mmHg with medication)
- evidence of vitreomacular traction (in either eye)
- active proliferative diabetic retinopathy (study eye)
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
visual acuity letter score
macular thickness(CST)
Arm Description
visual acuity letter score is used to compare between the two groups after interventional procedures
macular thickness(CST)is used to compare between the two groups after interventional procedures
Outcomes
Primary Outcome Measures
visual acuity letter score
The visual acuity letter score at one-year
central subfield thickness (CST)
the mean CST observed at one-year
Secondary Outcome Measures
patient compliant-complications
subjective symptoms
Full Information
NCT ID
NCT04186702
First Posted
November 30, 2019
Last Updated
December 4, 2019
Sponsor
Ain Shams University
1. Study Identification
Unique Protocol Identification Number
NCT04186702
Brief Title
New Concepts in Diabetic Macular Edema (DME)
Acronym
DME
Official Title
New Concepts in Diabetic Macular Edema (DME) Ranibizumab and Focal/Direct Laser for Chronic Diabetic Macular Edema With Vision Impairment
Study Type
Interventional
2. Study Status
Record Verification Date
December 2019
Overall Recruitment Status
Completed
Study Start Date
September 10, 2014 (Actual)
Primary Completion Date
October 1, 2016 (Actual)
Study Completion Date
September 9, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Intravitreal ranibizumab injection procedure is simple and effective. In management of chronic DME there is no clear anatomical endpoint. Visual stability is the primary aim. Argon focal laser therapy can be the safe second choice. The combined therapy is successful and practical for chronic DME patients.
Detailed Description
Settings and Design: Randomized clinical study
Subjects and Methods:
investigators randomly assigned 150 adults (the average age was 59.32 years ±2.79) with chronic diabetic macular edema involving the macular center for repeated ranibizumab injections (group A-75) or focal/direct argon laser after repeated ranibizumab injections (group B-75). The outcomes were the changes in visual acuity letter score and the central subfield thickness (CST) from baseline to one year. visual-acuity Letter score, and CST were analyzed with independent t-test and Mann Whitney-test. General linear model with multivariate analysis was used for visual acuity letter score, and CST in both groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, With Complications
Keywords
macula-injection- laser- ranibizumab-edema-thickness
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
interventional model
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
A clinical trial design strategy in which parties involved in the trial, the investigator and participants, do not know which participants have been assigned which interventions. Type of masking include: double-blind masking.
Allocation
Randomized
Enrollment
150 (Actual)
8. Arms, Groups, and Interventions
Arm Title
visual acuity letter score
Arm Type
Active Comparator
Arm Description
visual acuity letter score is used to compare between the two groups after interventional procedures
Arm Title
macular thickness(CST)
Arm Type
Active Comparator
Arm Description
macular thickness(CST)is used to compare between the two groups after interventional procedures
Intervention Type
Procedure
Intervention Name(s)
INTRAVITREAL RANIBIZUMAB INJECTION
Other Intervention Name(s)
focal/direct argon laser
Intervention Description
interventions involving RANIBIZUMAB INJECTION 0.5 mg (0.05 mL of 10 mg/mL solution)
Primary Outcome Measure Information:
Title
visual acuity letter score
Description
The visual acuity letter score at one-year
Time Frame
one-year follow up
Title
central subfield thickness (CST)
Description
the mean CST observed at one-year
Time Frame
one-year follow up
Secondary Outcome Measure Information:
Title
patient compliant-complications
Description
subjective symptoms
Time Frame
one-year follow up
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
focal maculopathy
diffuse macular edema
diffuse macular edema with ischemic changes
Exclusion Criteria:
ischemic maculopathy that was associated with grades of non-proliferative changes, or capillary drop out zones presented in the periphery of the macula
patients with history of stroke or transient ischemic attack
hypersensitivity to ranibizumab or any component of the ranibizumab formulation
uncontrolled glaucoma in either eye (intraocular pressure [IOP] >24 mmHg with medication)
evidence of vitreomacular traction (in either eye)
active proliferative diabetic retinopathy (study eye)
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Data processed and saved in eye center in the college
Learn more about this trial
New Concepts in Diabetic Macular Edema (DME)
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