The PresVIEW™ Procedure
Clinical research studies for PresVIEW™
Refocus Group is currently conducting clinical research studies using the PresVIEW™ Scleral Implant (PSI). These studies are designed to determine if implantation of the PSI device in the eye via the PresVIEW™ Procedure will:
- Reduce or eliminate the need for corrective eyewear arising from presbyopia; and/or,
- Reduce intraocular pressure (IOP) to help treat glaucoma and ocular hypertension (OHT).
See if you’re eligible to participate in one of Refocus’s studies.