Safety and Feasibility of the ELIOS System in POAG Patients

Last updated: June 13, 2025
Sponsor: Elios Vision, Inc.
Overall Status: Active - Recruiting

Phase

N/A

Condition

Glaucoma

Treatment

ELIOS Procedure

Clinical Study ID

NCT05999006
EP-02
  • Ages > 45
  • All Genders

Study Summary

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)

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Diagnosis of mild to moderate POAG

  • Medicated IOP of <=24 mmHg

  • Shaffer angle grade of III or IV

  • CD ratio <=0.8

  • At least 45 years old

Exclusion

Exclusion Criteria:

  • Closed-angle and secondary glaucomas

  • Prior incisional glaucoma surgery, intraocular surgery, or corneal surgery

  • Cannot undergo medication washout in the study eye

  • Diagnosis of degenerative visual disorders Non-study eye with BCVA worse than 20/80Known corticosteroid responder Pregnant or nursing women; or women of childbearingpotential not using medically acceptable birth control

Study Design

Total Participants: 65
Treatment Group(s): 1
Primary Treatment: ELIOS Procedure
Phase:
Study Start date:
October 18, 2023
Estimated Completion Date:
April 30, 2026

Connect with a study center

  • Elios Vision Clinical Site

    Glendale, Arizona 85306
    United States

    Active - Recruiting

  • Elios Vision Clinical Site

    Largo, Florida 33770
    United States

    Active - Recruiting

  • Elios Vision Clinical Site

    Rock Island, Illinois 61201
    United States

    Active - Recruiting

  • Elios Vision Clinical Site

    Oklahoma City, Oklahoma 73112
    United States

    Active - Recruiting

  • Elios Vision Clinical Site

    Kenosha, Wisconsin 53142
    United States

    Active - Recruiting

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