Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
iSTAR Medical
The goal of the registry is to collect data of the MINIject in a real-life setting. The registry has 3 main objectives: the collection of real-world evidence on the usability of the device, the patient reported outcomes, and the device safety over a period of 2 years after surgery.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
18+ years
diagnosed with open angle glaucoma, who has been or will be implanted with CE-marked MINIject
able to give consent
You may not be if
eyes with angle closure glaucoma
eyes with traumatic, malignant, uveitic or neovascular glaucoma or discernible congenital anomalies of the anterior chamber angle
patients with known intolerance or hypersensitivity to silicone
patients unable to give consent
Clareo Health | STAR-LIFE: a Post-market Registry on MINIject
