Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
iSTAR Medical
This Clinical Experience Program is being initiated to expand the surgical and clinical practice knowledge about the use of STARflo for reducing intraocular pression (IOP) in patients suffering from open angle glaucoma in a real world population of patients.
This program is designed to be an international multicenter observational study.
Patient data may be collected retrospectively and/or prospectively for up to 5 years after surgery.
The aim of this program is to document the patient's benefit following implantation of the STARflo implant in a real-word patient population, to learn about surgical practices and to collect data to support future cost-effectiveness analysis.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patients suffering from open angle glaucoma or some case of narrow angle glaucoma who have been implanted with STARflo implant from 2011
