Clinical Study Evaluating the Safety and Performance of the MIST Device for Intraocular Pressure Reduction in Patients With Primary Open-Angle Glaucoma

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40+
SponsorHexiris Inc

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)

Treatment groups

25 Participants
are divided into 1 treatment group

Sponsors and collaborators