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NCT05506423
Study of the CycloPen Micro-Interventional System and Long-Term Clinical Outcomes
Conditions: Open Angle Glaucoma
Sex: All
Ages: 21 Years – N/A
Healthy volunteers: No
Enrollment: 300
Sponsor: Iantrek, Inc.
Location: Visionary Eye Institute Newport Beach California
Summary
This observational study will enroll adults with open angle glaucoma (OAG) who had surgery to reduce intraocular pressure (IOP) using the CycloPen Micro-Interventional System. Consenting participants will be followed for 24 months after their surgery.
Data regarding IOP, use of glaucoma medications, and any side effects related to the surgery will be collected from participants' preoperative examination, their surgery, and postoperative examinations.
Eligibility Criteria
To be included, participants must have:
1. Open angle glaucoma
2. IOP-lowering surgical procedure using the CycloPen System
There are no exclusionary criteria.
Source: ClinicalTrials.gov (NCT05506423). StuddyBuddy aggregates publicly available trial information.
