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Comparison of Aflibercept Versus Ranibizumab in Management of Diabetic Macular Edema (DME)

Comparison of Aflibercept Versus Ranibizumab in Management of Diabetic Macular Edema

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04087746
Acronym
DME
Enrollment
400
Registered
2019-09-12
Start date
2017-01-31
Completion date
2019-06-30
Last updated
2019-09-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic Macular Edema

Brief summary

Diabetic macular edema (DME) is a sign of diabetic retinopathy that affects central vision. It is also a leading cause of visual decline in younger patients, especially in developing countries like our Arab community. Intra-vitrreal injection of anti-vascular endothelial growth factor (AVEGF) in management of DME had significant improvement in the final logMAR Un-corrected Distant Visual Acuity ( UCDVA) and logMAR Best Corrected Distant Visual Acuity (BCDVA), as well as reduction in the central retinal thickness from baseline measurement.

Detailed description

The investigators randomly assigned four hundreds eyes of diabetic patients with central diabetic macular edema for intra-vitreal injection of AVEGF group I (200 patients eyes) received aflibercept 2.0 mg and group II (200 patients eyes) received ranibizumab 0.3 mg. Injection was at 4 weeks interval according to the used protocol. The primary outcome was measuring the mean change in visual acuity as functional outcome and the secondary outcomes were the mean change in central macular thickness, as anatomical outcome rather than safety and efficacy of those two anti-VEGF drugs.

Interventions

DRUGAflibercept

Intra-vitreal injection of AVEGF AFLIBERCEPT in group I

DRUGRanibizumab

Intra-vitreal injection of AVEGF Ranibizumab in group 2

Sponsors

Minia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with type 1 or 2 diabetes mellitus with central DME clinically as well as documented by optical coherence tomography (OCT) imaging * The age of the patients at least 20 years old * Patients not receiving AVEGF injection, at least for one year * The BCDVA letter score of at least one eye (range, 0 to 115, with higher scores indicating better visual acuity of 90 (Snellen = 20/32) to 40 (Snellen = 20/320) and central DME .

Exclusion criteria

* Patients with cataract * Glaucoma patient * Previous AVEGF injection in less than one year * Patients not attending all of the scheduled follow up visits

Design outcomes

Primary

MeasureTime frameDescription
measuring the main change in visual acuity2 yearsmeasuring the main change in visual acuity in logarithm of the minimum angle of resolution (log MAR) using projector chart as functional outcome

Secondary

MeasureTime frameDescription
the main change in central macular thickness2 yearsthe main change in central macular thickness in micrometer by using optical coherence tomography (OCT) as anatomical outcome

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026