Actively Recruiting
Safety and Feasibility of the ELIOS System in POAG Patients
Led by Elios Vision, Inc. · Updated on 2025-06-17
65
Participants Needed
5
Research Sites
128 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Evaluation of the safety and effectiveness of the ELIOS System procedure to reduce intraocular pressure (IOP) in adult subjects with mild to moderate primary open-angle glaucoma (POAG)
CONDITIONS
Official Title
Safety and Feasibility of the ELIOS System in POAG Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of mild to moderate primary open-angle glaucoma
- Medicated intraocular pressure (IOP) of 24 mmHg or less
- Shaffer angle grade of III or IV
- Cup-to-disc ratio of 0.8 or less
- At least 45 years old
You will not qualify if you...
- Closed-angle and secondary glaucomas
- Prior incisional glaucoma surgery, intraocular surgery, or corneal surgery
- Unable to undergo medication washout in the study eye
- Diagnosis of degenerative visual disorders
- Non-study eye with best corrected visual acuity worse than 20/80
- Known corticosteroid responder
- Pregnant or nursing women, or women of childbearing potential not using medically acceptable birth control
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 5 locations
1
Elios Vision Clinical Site
Glendale, Arizona, United States, 85306
Actively Recruiting
2
Elios Vision Clinical Site
Largo, Florida, United States, 33770
Actively Recruiting
3
Elios Vision Clinical Site
Rock Island, Illinois, United States, 61201
Actively Recruiting
4
Elios Vision Clinical Site
Oklahoma City, Oklahoma, United States, 73112
Actively Recruiting
5
Elios Vision Clinical Site
Kenosha, Wisconsin, United States, 53142
Actively Recruiting
Research Team
R
Rupali Nangia
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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