Status: Recruiting
A Real-World Evidence Study of Goniotomy With the C-REX™ Instrument in Patients With Primary Open Angle Glaucoma
This study enrolls adults with primary open angle glaucoma (POAG) who underwent goniotomy intraocular pressure (IOP)-lowering surgery with the C-Rex Instrument. Patients are consented prior to surgery and followed for 12 months postoperatively. Data regarding IOP, use of glaucoma medications, and any device-related complications are collected during the study time period.
Participants needed: 200
Trial details
Age: 22+Biological sex: AllType: ObservationalSponsor: Iantrek, Inc.Updated: Mar 20, 2025Locations: 2Duration: 12 Months
Eligibility criteria
Primary open angle glaucoma [+1]
History of intraocular surgery within 8 weeks prior to C-Rex surgery [+3]