Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting NCT06984822 Sponsor: Vastra Gotaland Region Condition: Retinal Vein Occlusion and Diabetic Macular Oedema
Back to Retinal Vein Occlusion

Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting

NCT06984822
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with either Type 1 or Type 2 diabetes.
  • People who have diabetic swelling in the central part of the retina (the area responsible for sharp vision), where the swelling measures more than 280 microns thick and fluid-filled pockets are visible within the retinal layers.

Who may not be able to join:

  • People who have a history of any other disease affecting the central part of the retina.
  • People in the anti-VEGF treatment group who have received a dexamethasone implant (a slow-release steroid placed in the eye) within the last six months.
  • People in the dexamethasone implant group who have received anti-VEGF injections (a type of eye injection to reduce abnormal blood vessel growth) within the last two months.
  • People who have previously had surgery on the inside of the eye involving the gel or retina.
  • People who have previously had laser treatment applied to the central part of the retina.
  • People who have previously had a full laser treatment of the retina, which is used for advanced diabetic eye disease.
  • People who have had any eye surgery within the past three months.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Marita Grönlund, M.D. Prof, Göteborg University

Phone: +46738744867

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Vastra Gotaland Region
Registry
ClinicalTrials.gov
Start date
1 August 2025
Est. completion
31 December 2028

Where this trial is recruiting

🇸🇪 Sweden

Primary endpoints

Serum levels of Vascular Endothelial Growth Factor (VEGF); Serum levels of interleukin 6 (IL-6); Serum levels of interleukin 8 (IL-8); Serum levels of monocyte chemoattractant protein 1 (MCP-1); Serum levels of angiopoietin 2 (Ang-2); Serum levels of placental growth factor (PlGF); Serum levels of tumor necrosis factor alpha (TNF-a); Serum levels of intercellular adhesion molecule 1 (ICAM-1)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov