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Studying blood and eye scan markers in diabetic macular edema treatment

Compares blood and eye scan markers in people with diabetic macular edema receiving injected treatments.

Plain-language title generated from the registry record
Registry title: Evaluation of Serum- and OCT Biomarkers in Patients With DME Treated With Anti-VEGF or Dexamethasone Implant

Key facts

Where
Mölndal, SwedenSee the 2 sites

Where in Sweden

  • Ögonmottagning Mölndal/SUMölndal, SwedenNot yet recruiting
  • Sahlgrenska University Hospital, Department of OphthalmologyMölndal, SwedenTaking people

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Trial details

Who runs it
Vastra Gotaland Region
Trial code
NCT06984822
Record updated
21 November 2025
Original description
This study aims to investigate the association between serum biomarkers and clinical response to anti-VEGF or dexamethasone implant by assessing OCT-biomarkers in patients with diabetic macular edema, DME, and to compare these with a group of naive patients (those not previously treated for DME).Read full original descriptionShow less

Evaluation of Serum and Ocular Coherence Tomography Biomarkers in Patients With Diabetic Macular Edema Treated With Anti-VEGF or Dexamethasone Implant

This study aims to investigate the association between serum biomarkers and clinical response to anti-VEGF or dexamethasone implant by assessing OCT-biomarkers in patients with diabetic macular edema, DME, and to compare these with a group of naive patients (those not previously treated for DME).

Inclusion: Type I or type II DM; DME involving the center of the fovea with CFT more than 280 microns and the presence of intraretinal cysts.

Exclusion: Prior history of any other macular disease; Previous treatment with dexamethasone implants in the last six months for those in the anti-VEGF group; Previous treatment with anti-VEGF in the last two months for those in the dexamethasone implant group; Prior vitreoretinal surgery; Previous laser treatment of the macula; Previous panretinal photocoagulation; Ocular surgery in the previous 3 months.

ClinicalTrials.gov NCT06984822