Overview
As part of the post-market clinical follow-up (PMCF), this registry is developed to ensure real-world data collection on MINIject device.
Description
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.
Eligibility
Inclusion Criteria:
- 18+ years
- diagnosed with open angle glaucoma, who has been or will be implanted with CE-marked MINIject
- able to give consent
Exclusion Criteria:
- 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