Plain-English translation of NCT07359547 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This study doesn't follow the usual testing phases — it may be an observational study or a different type of research.
This trial is testing whether two different minimally invasive implants work equally well at lowering eye pressure in people with open-angle glaucoma. You would be randomly assigned to receive one of two devices—the XEN-63 Gel Stent or the PRESERFLO MicroShunt—during a single eye surgery. Researchers want to see which implant is most effective at controlling eye pressure over two years.
Open-angle glaucoma can lead to vision loss if eye pressure isn't controlled with medications alone. This study will help doctors understand whether these two newer surgical implants are effective alternatives for patients whose glaucoma isn't well controlled with eye drops.
You likely qualify if…
You likely don't qualify if…
You will have one surgical procedure to place either the XEN-63 Gel Stent or the PRESERFLO MicroShunt in your eye. After surgery, you'll attend regular follow-up visits over 24 months where doctors will measure your eye pressure, test your vision and visual field, take eye imaging scans, and check the health of your eye cells. You'll also report any side effects or additional treatments you receive during this time.
AI-generated summary from trial data · Jun 12, 2026 · Not medical advice
Belgium
Germany
Portugal