Clinical Study on the Efficacy of Oral Dapagliflozin Combined With Intravitreal Injection of Anti-Vascular Endothelial Growth Factor in Patients With Diabetic Macular Edema

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The purpose of this clinical study is to explore the efficacy of dapagliflozin as an adjunct to intravitreal anti-vascular endothelial growth factor (anti-VEGF) for enhanced reduction of retinal thickness and vision improvement in patients with diabetic macular edema. The main question the study aims to answer is: Does dapagliflozin reduce the thickness of the macula when combined with the standard of care intravitreal anti-VEGF therapy more than the intravitreal anti-VEGF therapy alone?

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• Type II diabetes mellitus patients, treated with premixed insulin and metformin, and diagnosed with center-involved diabetic macular edema (CiDME)

• Presence of retinal thickening involving the center of the fovea (CiDME) in the study eye on Optical Coherence Tomography (OCT) Heidelberg Spectralis; If both eyes are eligible, the eye with the greater central subfield thickness on OCT is selected as the study eye.

• Decreased visual acuity primarily attributable to DME

• Clear ocular media and pupillary dilation for adequate retinal imaging

• Ability to understand the study procedures and willingness to provide written informed consent

Locations
Other Locations
Egypt
Alexandria Main University Hospital, The Ophthalmology Department, Faculty of Medicine, Alexandria University
RECRUITING
Alexandria
Contact Information
Primary
Amira A. Nayel, Pharm.D, MSc
gs-amira.nayel@alexu.edu.eg
+201022715779
Time Frame
Start Date: 2025-02-08
Estimated Completion Date: 2026-08
Participants
Target number of participants: 56
Treatments
Experimental: Treatment group
The treatment group will receive oral dapagliflozin 10 mg daily in addition to standard of care intravitreal aflibercept injections.
Active_comparator: Control group
The control group will receive standard of care intravitreal aflibercept injections.
Sponsors
Leads: Alexandria University

This content was sourced from clinicaltrials.gov