search
Back to results

Lucentis for New Onset Neovascular Glaucoma (NVG)

Primary Purpose

Glaucoma, New Onset Glaucoma, Neovascular Glaucoma

Status
Withdrawn
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Ranibizumab (Lucentis)
Sponsored by
University of Illinois at Chicago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glaucoma focused on measuring glaucoma, neovascular glaucoma, new onset glaucoma, retinal ischemia, central retinal vein occlusion, proliferative diabetic retinopathy, ocular ischemic syndrome, carotid stenosis, vascular endothelial growth factor, neovascular

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Ability to provide written informed consent and comply with study assessments for the full duration of the study
  • Age > 21 years
  • Diagnosis of neovascular glaucoma (angle neovascularization with or without iris neovascularization and IOP > 21 mm Hg and > 5 mm Hg IOP compared to the fellow eye).
  • Neovascular glaucoma secondary to retinal ischemia (central retinal vein occlusion, proliferative diabetic retinopathy, ocular ischemic syndrome, etc.)

Exclusion Criteria:

  • Pregnancy (positive pregnancy test) or lactation or pre-menopausal women not using adequate contraception. The following are considered effective means of contraception: surgical sterilization or use of oral contraceptives, barrier contraception with either a condom or diaphragm in conjunction with spermicidal gel, an IUD, or contraceptive hormone implant or patch.
  • Prior enrollment in the study
  • Any other condition that the investigator believes would pose a significant hazard to the subject if the investigational therapy were initiated
  • Participation in another simultaneous medical investigation or trial
  • > 270 degrees of closed trabecular meshwork (closure secondary to peripheral anterior synechiae)
  • History of active inflammatory, infectious, or idiopathic keratitis precluding view of the anterior segment structures.
  • Previous intravitreal injections of ranibizumab or bevacizumab in either eye.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    1

    2

    Arm Description

    Lucentis (ranibizumab) with conventional treatment

    Conventional treatment

    Outcomes

    Primary Outcome Measures

    Mean change in best corrected visual acuity (BCVA) as assessed by the number of letters read correctly on the ETDRS eye chart at a starting test distance of 4 meters from baseline to Month 6.

    Secondary Outcome Measures

    Percent change in angle neovascularization (measured in clock hours by gonioscopy).
    Percent change in permanent angle closure (clock hours of peripheral anterior synechiae by gonioscopy).
    Mean change in intraocular pressure measured by applanation tonometry.
    Percent change in iris neovascularization (measured both in clock hours by slit lamp exam and with iris angiography).
    Rates of severe vision loss (visual acuity <20/200, loss of 6 lines or more on ETDRS chart).
    Number of intraocular pressure lowering medications needed to control intraocular pressure.
    Mean change in optic nerve cupping.
    Percent of patients requiring surgical glaucoma procedure to control intraocular pressure (trabeculectomy, seton, or ciliary body destruction).
    Percent of patients requiring pars plana vitrectomy with endolaser.
    Rates of endophthalmitis.
    Rates of rhegmatogenous retinal detachment.
    Final clock hours of permanent angle closure (clock hours of peripheral anterior synechiae by gonioscopy)

    Full Information

    First Posted
    July 29, 2008
    Last Updated
    February 13, 2020
    Sponsor
    University of Illinois at Chicago
    Collaborators
    Genentech, Inc.
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT00727038
    Brief Title
    Lucentis for New Onset Neovascular Glaucoma
    Acronym
    NVG
    Official Title
    Randomized Controlled Trial of Lucentis in the Management of New Onset Neovascular Glaucoma
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2008
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Company withdrew funding/sponsorship
    Study Start Date
    January 4, 2008 (Actual)
    Primary Completion Date
    May 15, 2009 (Actual)
    Study Completion Date
    May 15, 2009 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Illinois at Chicago
    Collaborators
    Genentech, Inc.

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Neovascular glaucoma is a potentially debilitating disease of the eye. Vascular eye disease such as diabetes and vein occlusions can cause the retina to release factors that promote the growth of abnormal blood vessels. These abnormal vessels can grow in the drainage mechanism of the eye causing pressure in the eye to markedly increase. This can potentially cause irreversible damage to the optic nerve from glaucoma leading to permanent blindness and painful eyes. Conventional treatments including laser and freezing therapy take weeks to cause regression in abnormal blood vessel growth. This delay often results in permanent vision loss and pain. New medications targeted at more immediately reducing blood vessel growth may aid in the treatment of this disease.
    Detailed Description
    Hypothesis: Intravitreal injection of Lucentis prior to conventional treatment for neovascular glaucoma improves overall outcome compared to conventional treatment alone. Specific Aims: To determine if pre-treatment with a single intravitreal injection of Lucentis prior to conventional treatment prevents severe vision loss and improves intraocular pressure control compared to conventional treatment alone. Neovascular glaucoma is a potentially devastating consequence of fibrovascular proliferation of the anterior chamber angle with subsequent obstruction of the trabecular meshwork. The production of peripheral anterior synechiae along the trabecular meshwork leads to progressive angle closure. The subsequent elevation in intraocular pressure is difficult to manage, often leading to rapid progression of glaucoma and significant loss of vision. Enucleation for blind, painful eyes secondary to neovascular glaucoma is not an uncommon sequelae. Neovascular glaucoma has many etiologic causes, the vast majority resulting from retinal ischemia secondary to relatively common diseases such as central retinal vein occlusion, proliferative diabetic retinopathy and ocular ischemic syndrome (carotid stenosis). (Sivac-Callcott et al., 2001) Vascular endothelial growth factor is likely a major contributor to the development of angle and iris neovascularization. (Ferrara, 2004) Although panretinal photocoagulation and/or cryoablation are mainstays of conventional treatment for neovascular glaucoma, the delayed therapeutic effect of these interventions often results in the formation of peripheral anterior synechiae and permanent angle closure. Recent limited case series have demonstrated a role for bevacizumab (Avastin) in reducing rubeosis iridis and as an adjunct for neovascular glaucoma. (Grisanti et al., 2006; Davidorf et al., 2006; Iliev et al., 2006; Kahook, Schuman, Noecker, 2006) However, no prospective studies have examined the potential utility of anti-vascular endothelial growth factor agents in the treatment of neovascular glaucoma. Intravitreal Lucentis is the standard of care for the treatment of exudative macular degeneration. Pharmacologic agents such as Lucentis, which selectively inhibit vascular endothelial growth factor may provide an important therapeutic adjunct for the treatment of neovascular glaucoma by more immediately causing regression of angle neovascularization and thereby providing a window for permanent treatment with laser or cryotherapy.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Glaucoma, New Onset Glaucoma, Neovascular Glaucoma, New Onset Neovascular Glaucoma
    Keywords
    glaucoma, neovascular glaucoma, new onset glaucoma, retinal ischemia, central retinal vein occlusion, proliferative diabetic retinopathy, ocular ischemic syndrome, carotid stenosis, vascular endothelial growth factor, neovascular

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1, Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Experimental
    Arm Description
    Lucentis (ranibizumab) with conventional treatment
    Arm Title
    2
    Arm Type
    No Intervention
    Arm Description
    Conventional treatment
    Intervention Type
    Drug
    Intervention Name(s)
    Ranibizumab (Lucentis)
    Other Intervention Name(s)
    ranibizumab, Lucentis
    Intervention Description
    0.5 mg ranibizumab intravitreal injection single dose administration
    Primary Outcome Measure Information:
    Title
    Mean change in best corrected visual acuity (BCVA) as assessed by the number of letters read correctly on the ETDRS eye chart at a starting test distance of 4 meters from baseline to Month 6.
    Time Frame
    Baseline to Month 6.
    Secondary Outcome Measure Information:
    Title
    Percent change in angle neovascularization (measured in clock hours by gonioscopy).
    Time Frame
    Initial visit through Month 6
    Title
    Percent change in permanent angle closure (clock hours of peripheral anterior synechiae by gonioscopy).
    Time Frame
    Initial visit through Month 6
    Title
    Mean change in intraocular pressure measured by applanation tonometry.
    Time Frame
    Initial visit through Month 6
    Title
    Percent change in iris neovascularization (measured both in clock hours by slit lamp exam and with iris angiography).
    Time Frame
    Initial visit through Month 6
    Title
    Rates of severe vision loss (visual acuity <20/200, loss of 6 lines or more on ETDRS chart).
    Time Frame
    Initial Visit through Month 6
    Title
    Number of intraocular pressure lowering medications needed to control intraocular pressure.
    Time Frame
    Initial Visit through Month 6
    Title
    Mean change in optic nerve cupping.
    Time Frame
    Initial Visit through Month 6
    Title
    Percent of patients requiring surgical glaucoma procedure to control intraocular pressure (trabeculectomy, seton, or ciliary body destruction).
    Time Frame
    Study duration
    Title
    Percent of patients requiring pars plana vitrectomy with endolaser.
    Time Frame
    Study duration
    Title
    Rates of endophthalmitis.
    Time Frame
    Study duration
    Title
    Rates of rhegmatogenous retinal detachment.
    Time Frame
    Study duration
    Title
    Final clock hours of permanent angle closure (clock hours of peripheral anterior synechiae by gonioscopy)
    Time Frame
    Month 6 visit

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    21 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Ability to provide written informed consent and comply with study assessments for the full duration of the study Age > 21 years Diagnosis of neovascular glaucoma (angle neovascularization with or without iris neovascularization and IOP > 21 mm Hg and > 5 mm Hg IOP compared to the fellow eye). Neovascular glaucoma secondary to retinal ischemia (central retinal vein occlusion, proliferative diabetic retinopathy, ocular ischemic syndrome, etc.) Exclusion Criteria: Pregnancy (positive pregnancy test) or lactation or pre-menopausal women not using adequate contraception. The following are considered effective means of contraception: surgical sterilization or use of oral contraceptives, barrier contraception with either a condom or diaphragm in conjunction with spermicidal gel, an IUD, or contraceptive hormone implant or patch. Prior enrollment in the study Any other condition that the investigator believes would pose a significant hazard to the subject if the investigational therapy were initiated Participation in another simultaneous medical investigation or trial > 270 degrees of closed trabecular meshwork (closure secondary to peripheral anterior synechiae) History of active inflammatory, infectious, or idiopathic keratitis precluding view of the anterior segment structures. Previous intravitreal injections of ranibizumab or bevacizumab in either eye.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Michael P Blair, MD
    Organizational Affiliation
    University of Illinois at Chicago
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    16508438
    Citation
    Avery RL. Regression of retinal and iris neovascularization after intravitreal bevacizumab (Avastin) treatment. Retina. 2006 Mar;26(3):352-4. doi: 10.1097/00006982-200603000-00016. No abstract available.
    Results Reference
    background
    PubMed Identifier
    16508439
    Citation
    Davidorf FH, Mouser JG, Derick RJ. Rapid improvement of rubeosis iridis from a single bevacizumab (Avastin) injection. Retina. 2006 Mar;26(3):354-6. doi: 10.1097/00006982-200603000-00017. No abstract available.
    Results Reference
    background
    PubMed Identifier
    15294883
    Citation
    Ferrara N. Vascular endothelial growth factor: basic science and clinical progress. Endocr Rev. 2004 Aug;25(4):581-611. doi: 10.1210/er.2003-0027.
    Results Reference
    background
    PubMed Identifier
    16854824
    Citation
    Fung AE, Rosenfeld PJ, Reichel E. The International Intravitreal Bevacizumab Safety Survey: using the internet to assess drug safety worldwide. Br J Ophthalmol. 2006 Nov;90(11):1344-9. doi: 10.1136/bjo.2006.099598. Epub 2006 Jul 19.
    Results Reference
    background
    PubMed Identifier
    17157590
    Citation
    Iliev ME, Domig D, Wolf-Schnurrbursch U, Wolf S, Sarra GM. Intravitreal bevacizumab (Avastin) in the treatment of neovascular glaucoma. Am J Ophthalmol. 2006 Dec;142(6):1054-6. doi: 10.1016/j.ajo.2006.06.066. Epub 2006 Aug 2.
    Results Reference
    background
    PubMed Identifier
    16583637
    Citation
    Kahook MY, Schuman JS, Noecker RJ. Intravitreal bevacizumab in a patient with neovascular glaucoma. Ophthalmic Surg Lasers Imaging. 2006 Mar-Apr;37(2):144-6.
    Results Reference
    background
    PubMed Identifier
    11581047
    Citation
    Sivak-Callcott JA, O'Day DM, Gass JD, Tsai JC. Evidence-based recommendations for the diagnosis and treatment of neovascular glaucoma. Ophthalmology. 2001 Oct;108(10):1767-76; quiz1777, 1800. doi: 10.1016/s0161-6420(01)00775-8.
    Results Reference
    background
    PubMed Identifier
    7487614
    Citation
    Results of the Endophthalmitis Vitrectomy Study. A randomized trial of immediate vitrectomy and of intravenous antibiotics for the treatment of postoperative bacterial endophthalmitis. Endophthalmitis Vitrectomy Study Group. Arch Ophthalmol. 1995 Dec;113(12):1479-96.
    Results Reference
    background
    Links:
    URL
    http://www.uic.edu/com/eye/
    Description
    University of Illinois at Chicago Eye and Ear Infirmary homepage

    Learn more about this trial

    Lucentis for New Onset Neovascular Glaucoma

    We'll reach out to this number within 24 hrs