Combined Intravitreal Bevacizumab With Topical Timolol-Dorzolamide Eye Drops in Diabetic Macular Edema
Primary Purpose
Diabetic Macular Edema
Status
Unknown status
Phase
Phase 2
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Injections of 1.25 mg of intravitreal bevacizumab with Timolol and Dorzolamide
Injections of 1.25 mg of intravitreal bevacizumab with artificial tears
Sponsored by
About this trial
This is an interventional treatment trial for Diabetic Macular Edema
Eligibility Criteria
Inclusion Criteria:
- Patients with Diabetic Melitus type 2
- Patients with center-involving diabetic macular edema (central macular edema > 300 micrometer)
- Patients have diabetic retinopathy at the stage of nonproliferative diabetic retinopathy (NPDR) or early PDR (proliferative diabetic retinopathy) or regressed PDR
- In patients with bilateral macular edema, only one eye is included in the study.
Exclusion Criteria:
- uncomplicated cataract surgery
- history of cataract surgery during last 4 months
- history of Panretinal Photocoagulation (PRP) during last 4 months
- any retinochoroidal disease except Diabetic retinopathy
- optic disc pathology
- patient with high-risk PDR or advanced PDR
- one-eye patients
- patient with glaucoma or uveitis
- pregnant or lactating patients
- patients whom topical Timolol or Dorzolamide are prohibited for any reason
Sites / Locations
- Ophthalmic Research Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Injections of 1.25 mg of intravitreal bevacizumab with topical drops of Timolol and Dorzolamide
Injections of 1.25 mg of intravitreal bevacizumab with artificial tears
Arm Description
31 cases in intervention group receive injections of 1.25 mg of intravitreal bevacizumab monthly for 3 months (months 0, 1 and 2) with topical drops of Timolol twice a day and Dorzolamide twice a day
31 cases in control group receive intravitreal injection of 1.25 mg bevacizumab monthly for 3 months (months 0, 1 and 2) plus artificial tears (twice a day as a placebo)
Outcomes
Primary Outcome Measures
Central macular thickness
Measured by EDI-OCT
Secondary Outcome Measures
Best corrected visual acuity (BCVA)
By ophthalmology resident with subjective and objective refraction
Full Information
NCT ID
NCT05083689
First Posted
October 6, 2021
Last Updated
October 6, 2021
Sponsor
Shahid Beheshti University of Medical Sciences
1. Study Identification
Unique Protocol Identification Number
NCT05083689
Brief Title
Combined Intravitreal Bevacizumab With Topical Timolol-Dorzolamide Eye Drops in Diabetic Macular Edema
Official Title
Combined Intravitreal Bevacizumab With Topical Timolol-Dorzolamide Eye Drops in Diabetic Macular Edema
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
October 6, 2021 (Actual)
Primary Completion Date
March 2022 (Anticipated)
Study Completion Date
April 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shahid Beheshti University of Medical Sciences
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
This study is a double-blind randomized clinical trial in Diabetic patients (type 2) over 18 years of age who have diabetic macular edema with involvement of the central 1 millimeter (central macular thickness is more than 300 μm) and BCVA 20/30 or less who visit the retina clinic of Labbafinejad Hospital Are studied. (In patients with bilateral macular edema, only one eye is included in the study.) Complete ocular examinations (including best corrected visual acuity - anterior segment - intraocular pressure - dilated pupil funduscopy with severity of diabetic retinopathy), optical coherence tomography (OCT), EDI-OCT( Enhanced Depth Imaging Optical Coherence Tomography ) - as well as Optical coherence tomography angiography (OCTA ) are performed for all patients at baseline. Blood tests are also taken from patients for fasting blood sugar and HbA1C. Patients are then randomly divided into two groups. The first group is treated with injections of 1.25 mg of intravitreal bevacizumab monthly for 3 months (months 0, 1 and 2) with topical drops of Timolol twice a day and Dorzolamide twice a day. For the second group (control group), 3 injections of 1.25 mg of intravitreal bevacizumab monthly with artificial tears (twice a day as a placebo) are prescribed. Patients in both groups are visited 1 month after the third basic intravitreal bevacizumab (IVB) injection and complete ophthalmology examinations are performed and central thickness of macula is recorded based on the patient's OCT as well as the need for IVB re-injection. EDI (Enhanced Depth Imaging)-OCT and OCTA are performed again for all patients.
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
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
62 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Injections of 1.25 mg of intravitreal bevacizumab with topical drops of Timolol and Dorzolamide
Arm Type
Active Comparator
Arm Description
31 cases in intervention group receive injections of 1.25 mg of intravitreal bevacizumab monthly for 3 months (months 0, 1 and 2) with topical drops of Timolol twice a day and Dorzolamide twice a day
Arm Title
Injections of 1.25 mg of intravitreal bevacizumab with artificial tears
Arm Type
Placebo Comparator
Arm Description
31 cases in control group receive intravitreal injection of 1.25 mg bevacizumab monthly for 3 months (months 0, 1 and 2) plus artificial tears (twice a day as a placebo)
Intervention Type
Drug
Intervention Name(s)
Injections of 1.25 mg of intravitreal bevacizumab with Timolol and Dorzolamide
Intervention Description
31 cases in intervention group receive injections of 1.25 mg of intravitreal bevacizumab monthly for 3 months (months 0, 1 and 2) with topical drops of Timolol twice a day and Dorzolamide twice a day
Intervention Type
Drug
Intervention Name(s)
Injections of 1.25 mg of intravitreal bevacizumab with artificial tears
Intervention Description
31 cases in control group receive intravitreal injection of 1.25 mg bevacizumab monthly for 3 months (months 0, 1 and 2) plus artificial tears (twice a day as a placebo)
Primary Outcome Measure Information:
Title
Central macular thickness
Description
Measured by EDI-OCT
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Best corrected visual acuity (BCVA)
Description
By ophthalmology resident with subjective and objective refraction
Time Frame
1 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients with Diabetic Melitus type 2
Patients with center-involving diabetic macular edema (central macular edema > 300 micrometer)
Patients have diabetic retinopathy at the stage of nonproliferative diabetic retinopathy (NPDR) or early PDR (proliferative diabetic retinopathy) or regressed PDR
In patients with bilateral macular edema, only one eye is included in the study.
Exclusion Criteria:
uncomplicated cataract surgery
history of cataract surgery during last 4 months
history of Panretinal Photocoagulation (PRP) during last 4 months
any retinochoroidal disease except Diabetic retinopathy
optic disc pathology
patient with high-risk PDR or advanced PDR
one-eye patients
patient with glaucoma or uveitis
pregnant or lactating patients
patients whom topical Timolol or Dorzolamide are prohibited for any reason
Facility Information:
Facility Name
Ophthalmic Research Center
City
Tehran
Country
Iran, Islamic Republic of
12. IPD Sharing Statement
Learn more about this trial
Combined Intravitreal Bevacizumab With Topical Timolol-Dorzolamide Eye Drops in Diabetic Macular Edema
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