Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting
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 are older than 18 years of age
- People who have been diagnosed with either Type 1 or Type 2 Diabetes and have recently been diagnosed with a condition called Proliferative Diabetic Retinopathy (PDR), which is an advanced stage of diabetic eye disease
- People whose vision meets a minimum level of sharpness, measured on a standard eye chart (confirm with trial site for exact threshold)
- People whose retina (the light-sensitive layer at the back of the eye) measures less than 300 micrometres in thickness on a special scan called an OCT, with no fluid-filled pockets (cysts) present
- People whose eye is clear enough and whose pupil can be dilated wide enough to allow a type of laser eye treatment called PRP (Panretinal Photocoagulation)
Who may not be able to join:
- People who have had eye surgery in the past 4 months, or who have eye surgery planned within the next 3 months
- People who have had, or currently have, a condition where diabetic swelling affects the central part of the retina (called centre-involved diabetic macular oedema)
- People whose eye being studied has previously received PRP laser treatment, injections into the eye, or laser treatment to the central retina area
- People who are taking medications known to increase the risk of swelling in the retina
- People whose eye has cloudiness or other issues that would prevent the laser treatment from being delivered properly
- People whose general health makes it very difficult or impossible to receive laser treatment in a clinic setting
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.
Contact this trial
Principal Investigator: Marita Andersson 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
Where this trial is recruiting
Primary endpoints
Central subfield retinal thickness (CRT); Vessel Perfusion Density (VPD); Vessel Length Density (VLD); Foveal Avascular Zone (FAZ); Lesion size; Macular volume; Venular saturation; Arteriolar saturation; Retinal diameter; Venular diameter; Retinal function; Diabetic macular edema (DME); Subjective experience of pain after treatment; Subjective overall experience of the treatment; Cost-effectiveness
Can't join this trial?
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.