Image

Randomized Clinical Trial to Evaluate the Effect of Dapagliflozin in Patients With Diabetic Macular Edema

Randomized Clinical Trial to Evaluate the Effect of Dapagliflozin in Patients With Diabetic Macular Edema

Recruiting
18-85 years
All
Phase 2

Powered by AI

Overview

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?

Description

Some evidence in the literature suggests that sodium glucose co-transporter 2 (SGLT2) inhibitors may be beneficial in reducing diabetic macular edema. The objective of this clinical trial is to investigate the efficacy and safety of dapagliflozin when combined with intravitreal aflibercept injections in the management of patients with type II diabetes mellitus and center-involved diabetic macular edema (ci-DME). This randomized, double-blind, parallel group, active control design, clinical trial, is investigating the effect of oral dapagliflozin 10 mg given once daily in addition to intravitreal aflibercept versus intravitreal aflibercept alone on reducing macular central subfield thickness (CST) and improving visual acuity in diabetic patients with ci-DME.

Eligibility

Inclusion criteria:

  • 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

Study participant exclusion criteria:

  • Patients below 18 years old and patients above 85 years old
  • Patients with type I diabetes mellitus (Insulin dependent diabetes mellitus IDDM)
  • Pregnant women and lactating women diagnosed with diabetes or intending to become pregnant in the next 12 months
  • Patients who had myocardial infarction within 3 months prior to screening
  • Patients who had transient ischemic attack (TIA), ischemic or hemorrhagic stroke within 3 months prior to screening
  • Patients with poorly controlled diabetes mellitus, defined as patients having glycosylated hemoglobin (HbA1c) level of ≥12% at screening or patients who were hospitalized for diabetic ketoacidosis or hyperosmolar coma within 4 months prior to screening
  • Patients with estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m2 at screening
  • Patients with severe hepatic impairment of Child-Turcotte-Pugh class C at screening
  • Patients treated with antidiabetic drugs thiazolidinediones (TZD) (rosiglitazone and pioglitazone) prior to screening
  • Patients who were receiving SGLT2 inhibitors (e.g., dapagliflozin, canagliflozin, or empagliflozin) within 3 months prior to screening
  • Known allergy or hypersensitivity to any component of the study drugs
  • Current or previous participation in another clinical study involving the systemic or ocular administration of an investigational drug or device within 6 months of screening

Study eye exclusion criteria:

  • Macular edema caused by other conditions than diabetic macular edema or coexisting with DME such as retinal vein occlusion, choroidal neovascularization (CNV), or uveitic cystoid macular edema
  • History of postoperative cystoid macular edema (Irvine-Gass syndrome)
  • Cataract extraction within 3 months prior to screening
  • Patients who had previous macular laser treatment
  • Patients who had peripheral panretinal photocoagulation laser (PRP) treatment within 6 months prior to screening
  • Patients who have been treated with intravitreal anti-VEGF or intravitreal corticosteroids within 6 months prior to screening
  • The use of corticosteroids or non-steroidal anti-inflammatory eye drops within 1 month prior to screening
  • Patients on topical prostaglandin analogs (e.g., latanoprost, travoprost, ioprost, or tafluprost) at screening
  • History of vitrectomy or scleral buckling
  • Presence of diffuse vitreomacular traction or thick epiretinal membrane on OCT causing significant traction
  • Presence of tractional retinal detachment involving the macula and requiring vitrectomy
  • Presence of other associated macular pathology (e.g., macular scars or macular holes) on OCT
  • Presence of rubeosis iridis
  • Signs of hypertensive retinopathy (arterioral spasm or silver wiring of blood vessels)
  • Presence of glaucoma
  • Aphakia
  • Yttrium aluminum garnet (YAG) laser capsulotomy within 3 months prior to screening
  • Patients diagnosed with ocular surface infections until treated prior to receiving the intravitreal injections

Non-study eye exclusion criteria:

• The non-study eye receiving simultaneous intravitreal anti-VEGF treatment with the study eye

Study details
    Diabetic Macular Edema
    Center-involved Diabetic Macular Edema

NCT06845163

Alexandria University

15 October 2025

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.