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Withdrawn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
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
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
NCT ID
NCT00727038
First Posted
July 29, 2008
Last Updated
February 13, 2020
Sponsor
University of Illinois at Chicago
Collaborators
Genentech, Inc.
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