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NCT06985706From ClinicalTrials.govRecruiting

Anti-vascular Endothelial Growth Factor (Anti-VEGF) Monotherapy vs Anti-VEGF Followed by Subthreshold Micropulse Laser for Treating Severe Diabetic Macular Oedema When the Central Retina Goes <400 Microns

Treatment of Severe Diabetic Macular Oedema With Anti-vascular Endothelial Growth Factor (Anti-VEGF) Monotherapy vs Anti-VEGF Followed by Subthreshold Micropulse Laser When the Thickness of the Central Retina Goes Below 400 Microns: Pragmatic Randomised Equivalence Trial

  • Severe Diabetic Macular Oedema

At a glance

Phase
Phase 3
Study type
Interventional
Sponsor
Belfast Health and Social Care Trust
Enrolment target
264
Started
19 May 2025
Main results due
30 November 2028
Study sites
22
Registry updated
28 September 2026

Can you take part?

  • Aged 18 years and over.
  • Open to any sex.
  • You need the condition being studied — healthy volunteers are not accepted.

These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.

Read the full eligibility criteria
Inclusion Criteria:

* Adults (\>18 years)
* Diabetes type 1 or type 2
* Presented with severe centre-involving (CI)-DMO (CRT ≥400 μm)
* Within the first year of initiating anti-VEGF therapy but who still have DMO and their CRT is below 400 μm (and it remains, at the time of randomisation) following anti-VEGF therapy in either one eye or both eyes

Exclusion Criteria:

* Causes of macular oedema other than DMO
* DMO with CRT ≥400 μm
* Receipt of anti-VEGFs before their presentation with severe DMO (previous macular laser treatment for DMO is allowed)
* Use of unlicensed anti-VEGFs (e.g. bevacizumab)
* Inability, for any reason, to attend study visits
* Active proliferative diabetic retinopathy (PDR) (treated and inactive PDR is allowed)
* Use of pioglitazone which cannot be stopped for the duration of the trial
* Cataract surgery or laser pan-retinal photocoagulation (PRP) within the previous 6 weeks
* Currently enrolled in a Clinical Trial of an Investigational Medical Product
* Declined consent for participation

What this study is about

In the sponsor’s own words, from the registry.

The macula is the centre of the retina; it gives central sight, colour and fine detail. People with diabetes may develop diabetic macular oedema (DMO). In DMO, fluid leaks from blood vessels and builds up at the macula, causing sight loss. DMO can be mild or severe; this is determined by measuring, in microns (µm), how thick the macula is. One µm is one-thousandth of a millimetre. People presenting with mild DMO (macula less than 400 µm thick; normally it is around 250 µm but varies with sex and ethnicity) are offered macular laser treatment. Laser works well for these patients. Subthreshold micropulse laser (SML), which does not damage the macula, works as well as standard laser, which produces a burn, and is cost-effective. However, many people present with severe DMO (macula 400 µm or thicker) where the laser does not work well. The standard treatment is eye injections of anti-VEGFs. VEGF stands for vascular endothelial growth factor. VEGF is high in eyes with DMO and causes blood vessel leakage. Anti-VEGFs block VEGF. They are given monthly to begin with, then every 2-3 months for months or years until DMO clears. In many patients DMO comes back after clearing and anti-VEGFs need to be re-started most often monthly initially again. To improve the care of people with severe DMO this study will compare the current standard care (anti-VEGFs alone) with a strategy in which patients begin with an anti-VEGF but switch to SML once the macula is less than 400 µm thick.

Patients aged over 18 years with type 1 or type 2 diabetes and severe DMO can participate. They are randomly allocated either anti-VEGFs alone or anti-VEGFs then SML when the macula is less than 400 µm thick.

Study sites(22)

  • Bedford Hospital

    Bedford, United Kingdom

    Recruiting

  • The Royal Hospitals Belfast

    Belfast, United Kingdom

    Recruiting

  • Birmingham and Midland Eye Centre

    Birmingham, United Kingdom

    Recruiting

  • Sussex Eye Hospital

    Brighton, United Kingdom

    Recruiting

  • Bristol Eye Hospital

    Bristol, United Kingdom

    Recruiting

  • Frimley Park Hospital

    Camberley, United Kingdom

    Recruiting

  • University Hospital of Wales

    Cardiff, United Kingdom

    Not yet recruiting

  • Gloucestershire Royal Hospital

    Gloucester, United Kingdom

    Recruiting

  • Hull Royal Infirmary

    Hull, United Kingdom

    Recruiting

  • Royal Liverpool University Hospital

    Liverpool, United Kingdom

    Recruiting

  • Central Middlesex Hospital

    London, United Kingdom

    Recruiting

  • Chelsea and Westminster Hospital

    London, United Kingdom

    Recruiting

  • Kings College Hospital

    London, United Kingdom

    Recruiting

  • Moorfields Eye Hospital

    London, United Kingdom

    Recruiting

  • James Cook Hospital

    Middlesbrough, United Kingdom

    Recruiting

  • Royal Gwent Hospital

    Newport, United Kingdom

    Recruiting

  • Queen's Medical Centre

    Nottingham, United Kingdom

    Not yet recruiting

  • University Hospital Southampton

    Southampton, United Kingdom

    Recruiting

  • Sunderland Eye Hospital

    Sunderland, United Kingdom

    Recruiting

  • Singleton Hospital

    Swansea, United Kingdom

    Recruiting

  • Torbay Hospital

    Torquay, United Kingdom

    Recruiting

  • Hillingdon Hospital

    Uxbridge, United Kingdom

    Recruiting

Showing 22 of 22 sites. 20 of the 22 sites on this study are recruiting right now — a site can stop enrolling while the study as a whole is still open.

Source: ClinicalTrials.gov record NCT06985706. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.

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Anti-vascular Endothelial Growth Factor (Anti-VEGF) Monotherapy vs Anti-VEGF Followed by Subthreshold Micropul | Trialion