About this trial
It is an interventional study for the treatment of Primary Open-Angle Glaucoma (POAG) using the Hexiris Microinvasive Scleral Trephine (MIST) system. This medical device includes a sclerectomy punch and injector assembly. It is a multicenter, open-label, non-randomized, single-arm study. Adults aged 40 years or more will be enrolled if the POAG is inadequately controlled by topical drug therapies. Only one eye per subject will be treated. The study will be performed on the first five patients in the operating room and the subsequent 20 patients will be treated under a slit-lamp in an aseptic environment (external patient clinic).Once treated with the MIST device, patients will return the next day, 1 week later and 1, 2, 3, 6, 9 and 12 months later. During these follow-up visits, the ophthalmologist will examine the eye and take measurements of the intraocular pressure.
Eligibility criteria
Qualifiers
Adults ≥ 40 years with uncontrolled mild to moderate POAG.
IOP ≥ 18 mmHg on ≥1 topical IOP-lowering medications.
Open angle on gonioscopy
Clear cornea and healthy ocular surface
Disqualifiers
Prior glaucoma filtering surgery (trabeculectomy, shunt or valve) in the treatment quadrant
Angle-closure, neovascular, uveitic, or traumatic glaucoma.
Eyes with conjunctival scarring, prior conjunctival surgery or other pathologies in the treatment quadrant
Eyes with scleral thinning, staphyloma, or structural abnormalities in the treatment quadrant
Trial design
Treatments tested in this trial
- Hexiris Microinvasive Scleral Trephine (MIST)