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Clinical Trial

A Real-World Evidence Study of Goniotomy With the C-REX™ Instrument in Patients With Primary Open Angle Glaucoma

NCT: NCT06615661 · ACTIVE_NOT_RECRUITING

NCT IDNCT06615661
StatusACTIVE_NOT_RECRUITING
Start Date2024-08-14
SponsorIantrek, Inc. (INDUSTRY)
First posted
Last updated

Brief Summary

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.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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