OMNIgl: Standalone OMNI Surgical System for Open-angle Glaucoma

Sponsor
Iqbal Ahmed (Other)
Overall Status
Terminated
CT.gov ID
NCT04427995
Collaborator
OMNI Medical Services, LLC (Other)
30
1
24.2
1.2

Study Details

Study Description

Brief Summary

The emergence of minimally invasive glaucoma surgeries (MIGS) has seen a variety of potential innovative surgical alternatives to help better control intraocular pressure (IOP). The OMNI™ Surgical System (Sight Sciences, Menlo Park, CA, USA) is a promising MIGS procedure. It combines two procedures known as trabeculotomy and viscodilation of Schlemm's canal in one hand held device without the need for additional incisions or extra instrumentation. The device recently received FDA approval in the United States for certain indications in ophthalmic surgery. To date, no study has examined the effect of standalone viscodilation and trabeculotomy on glaucoma drop burden and IOP.

Condition or Disease Intervention/Treatment Phase
  • Device: OMNI surgical system

Detailed Description

The emergence of minimally invasive glaucoma surgeries (MIGS) has seen a variety of potential innovative surgical alternatives to help better control intraocular pressure (IOP).1 The OMNI™ Surgical System (Sight Sciences, Menlo Park, CA, USA) is a promising procedure which targets the conventional outflow pathway.2 This device treats the trabecular meshwork, Schlemm's canal and the distal collector channels, all conventional pathway points of aqueous outflow resistance. Its designed microcatheter allows for cannulation of Schlemm's canal, dilation using the controlled delivery of viscoelastic as well as a trabeculotomy by stripping the trabecular meshwork will retracting the catheter.3 Goniotomy-assisted transluminal trabeculotomy (GATT) has shown promising results in using an ab interno approach to cleave the trabecular meshwork.4 Alternatively, viscodilation alone has also shown an IOP lowering effect. 5 The OMNI Surgical System combines both procedures in one hand held device without the need for additional incisions or extra instrumentation. The device recently received FDA approval in the United States for delivery of small amounts of viscoelastic fluid during ophthalmic surgery and to cut trabecular meshwork tissue during trabeculotomy procedures.6 To date, no study has examined the effect of standalone viscodilation and trabeculotomy on glaucoma drop burden and IOP.

Study Design

Study Type:
Observational
Actual Enrollment :
30 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Standalone OMNI Surgical System for Open-angle Glaucoma
Actual Study Start Date :
Mar 25, 2019
Actual Primary Completion Date :
Mar 31, 2021
Actual Study Completion Date :
Apr 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Oen Angle Glaucoma

• Patients aged 30-95 with primary or pigmentary / pseudoexfolliative / juvenile / normal pressure open angle glaucoma or combined mechanism glaucoma with IOP of 10-40 mmHg on maximum tolerated medical therapy who are either progressing, above IOP target, or poorly adherent or tolerant to medical therapy. Phakic or pseudophakic eyes and previous laser trabeculoplasty will be included.

Device: OMNI surgical system
GATT + viscodilation
Other Names:
  • OMNI surgical systems
  • Outcome Measures

    Primary Outcome Measures

    1. Lower Intraocular Pressure and medication dependence [Postoperative week 1, month 1, month 3, annually]

      Change in IOP less than or equal to baseline with a medication reduction to 1 or less or an IOP change of 20% or less from baseline with medication

    Secondary Outcome Measures

    1. Examine the adverse event profile of the OMNI surgical system in patients with open angle glaucoma. [1 month post operatively]

      Absence of the following complications: 1. ) Starting after POM1: shallow AC w/ iridocorneal touch, any hyphema, corneal edema, wound leak/dehiscience, choroidal effusion, malignant glaucoma, dellen/non-healing epithelial defect, ptosis, diplopia, and/or; 2.) At any point: additional glaucoma surgery, loss of light perception vision, vitreous hemorrhage, ≥2mm hyphema, hypotony maculopathy, macular edema, choroidal effusion/hemorrhage requiring drainage, suprachoroidal hemorrhage, retinal detachment, endophthalmitis

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 95 Years
    Sexes Eligible for Study:
    All

    Inclusion Criteria

    • Patients aged 30-95 with primary or pigmentary / pseudoexfolliative / juvenile / normal pressure open angle glaucoma or combined mechanism glaucoma.

    • An IOP of 10-40 mmHg on maximum tolerated medical therapy who are either progressing, above IOP target, or poorly adherent or tolerant to medical therapy.

    • Phakic or pseudophakic eyes and previous laser trabeculoplasty will be included.

    Exclusion Criteria:
    • Other forms of glaucoma,

    • prior incisional glaucoma surgery,

    • prior corneal graft (PKP, DALK, DSAEK, DMEK),

    • Shafer angle grading <2 in 2 or more quadrants.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Prism Eye Institute Oakville Ontario Canada L6H 0J8

    Sponsors and Collaborators

    • Iqbal Ahmed
    • OMNI Medical Services, LLC

    Investigators

    • Principal Investigator: Iqbal Ahmed, MD, Prism Eye Institute

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Iqbal Ahmed, Principal Investigator, Prism Eye Institute
    ClinicalTrials.gov Identifier:
    NCT04427995
    Other Study ID Numbers:
    • 948
    First Posted:
    Jun 11, 2020
    Last Update Posted:
    Jul 26, 2021
    Last Verified:
    Jul 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 26, 2021