Comparing XEN®-63 Gel Stent and PRESERFLO® MicroShunt
Recruiting
N/A
Interventional Study
GLAUCOMA 1, OPEN ANGLE, D (Disorder)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 40 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 166 (estimated)
- Sponsor
- Universitaire Ziekenhuizen KU Leuven · Other
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About This Trial
The goal of this randomized controlled clinical trial is to learn whether two minimally invasive bleb-forming glaucoma implants can effectively treat adult patients with open-angle glaucoma who require surgical lowering of intraocular pressure (IOP). Specifically, the study evaluates whether the PRESERFLO™ MicroShunt is at least as effective as the XEN®-63 Gel Stent in reducing IOP after surgery. …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* \>40 years of age
* An established diagnosis of: Primary open angle glaucoma, Normal tension glaucoma, Pigment dispersion glaucoma (PDG) or Pseudoexfoliative glaucoma (PEX)
* Inadequately controlled on maximum tolerated medical therapy.
* Mean Deviation (MD) \</= -3
* Intraocu…
Contacts