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Completed

NCT Number: NCT01951066

Diabetic Macular Edema Treated With Ozurdex (DMEO)

To measure various pro-permeability factors in the aqueous humor of patients with persistent/recurrent diabetic macular edema

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Wilmer Eye Institute

Baltimore, Maryland, 21287, United States

About this study

Patients with Diabetic Macular Edema (DME) are increasingly being treated with molecules targeting vascular endothelial factor (VEGF). One potential advantage of a dexamethasone implant over specific VEGF antagonists is that steroids suppress production of multiple pro-permeability factors.

Our primary objective is to measure the pro-permeability factors in the aqueous humor of patients with persistent/recurrent macular edema despite prior treatment with anti-VEGF agents at baseline and at 1, 2, 3, and 4 months after intraocular injection of a dexamethasone implant.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • • Signed informed consent and authorization of use and disclosure of protected health information
  • Age more than or equal to 18 years
  • Diagnosis of diabetic macular edema
  • Intraretinal or subretinal fluid in the macula determined by Spectralis OCT
  • Best corrected visual acuity score in the study eye of 20/30 to 20/400 inclusive (Snellen equivalents using the ETDRS protocol at a distance of 4 meters)
  • In the opinion of the investigator, decreased vision in the study eye is due to foveal thickening from DME and not from other obvious causes of decreased vision
  • Persistent or recurrent edema despite prolonged treatment with an anti-VEFG agent

Exclusion criteria

  • • Scatter laser photocoagulation or macular photocoagulation within 3 months of study entry in the study eye
  • Intraocular surgery in the study eye within 3 months of study entry
  • Use of intraocular or periocular injection of steroids in the study eye (e.g., triamcinolone) within 4 months of study entry
  • Previous use of an anti-VEGF drug within 1 month of study entry
  • Yttrium-Aluminum-Garnet (YAG) laser capsulotomy within 1 month of study entry
  • Any condition that the investigator believes would pose a significant hazard to the subject if investigational therapy were initiated.
  • Inability to comply with study or follow up procedures
  • History of glaucoma. (Patients who have undergone filtration surgery may be included)
  • Patients with active or suspected ocular or periocular infection, including most viral diseases of the cornea and conjunctiva, including active epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, varicella, mycobacterial infections, and fungal diseases.
  • Aphakic eyes with rupture of the posterior lens capsule.
  • Eyes with ACIOL and rupture of the posterior lens capsule.
  • Patients with hypersensitivity to dexamethasone or to any other components of the product

Treatment and study plan

Dexamethasone implant

Drug

Patients will receive a single injection of a dexmethasone implant

Anti-VEGF injection

Drug

Patients will receive PRN injections of an anti-VEGF agent

Primary outcomes

  1. Correlation Between Change in Level of Propermeability Factors With Change in Edema After Treatment With a Dexamethasone Implant or Anti-VEGF Agent

    Time frame: 1, 2, 3, and 4 months after injection of a dexamethasone implant or anti-VEGF agent

    Changes in propermeability factor levels were correlated with changes in edema using the person correlation coefficient (this was calculated using data from all time points).

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Registry information

Acronym: DMEO

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Sep 26, 2013
Registry last updated
Sep 29, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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