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Trabeculectomy With Mitomycin C Associated With Sub-conjunctival Injection of Ranibizumab

Trabeculectomy With Mitomycin C Associated With Sub-conjunctival Injection of Ranibizumab

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00892398
Enrollment
242
Registered
2009-05-04
Start date
2009-03-31
Completion date
2014-03-31
Last updated
2014-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma

Keywords

Trabeculectomy, Vascular Endothelial Growth Factor A, Wound Healing, Angiogenesis Inhibitors

Brief summary

Trabeculectomy with mitomycin C remains the standard surgery for glaucoma. This surgery involves creating a door in the eye wall in order to improve fluid outflow and decrease intraocular pressure. However, success rates range from 70% to 90% depending on the criteria used and tend to decrease with time. The failure of the surgery is associated with inflammation, new blood vessel formation and scarring which can cause closure of the door. Molecules which inhibit new blood vessel formation such as inhibitors of vascular endothelial growth factor have been used successfully to decrease scarring in animal eyes where little doors were created and significantly improve survival. Furthermore, they have shown promise when used during trabeculectomy. Ranibizumab, a vascular endothelial growth factor, has also been used safely in intraocular surgery to treat other diseases which involve new blood vessel formation such as macular degeneration and diabetes. The investigators hypothesize that ranibizumab may decrease the failure rate of trabeculectomy with mitomycin C by decreasing scarring. The aim of the study is to evaluate the difference in failure rates and bleb morphology at one year post-operatively in eyes having undergone sub-conjunctival injections of ranibizumab in addition to primary trabeculectomy with mitomycin C compared to eyes having undergone trabeculectomy with mitomycin C alone.

Detailed description

Prospective, randomized, unblinded clinical trial. Two groups of patients with glaucoma undergoing primary trabeculectomy or phaco-trabeculectomy with MMC between March 2009 and September 2012. The ranibizumab group (RAN) received 2 subconjunctival injections of 0.5 mg of ranibizumab (intraoperatively and on day 14) and he control group did not receive ranibizumab.

Interventions

DRUGranibizumab

Two ranibizumab subconjunctival injections (0.5 mg ∕ 0.05 mL). The first injection at the end of the surgery (intraoperative) and the second two weeks post-operatively.

PROCEDUREstandard care

standard post-operative care after trabeculectomy with mitomycin C

Sponsors

Novartis
CollaboratorINDUSTRY
Maisonneuve-Rosemont Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* to have uncontrolled glaucoma * to have accepted to undergo a primary trabeculectomy with mitomycin C * to have one of the following types of glaucoma: * Normal tension Glaucoma * Chronic Open-Angle Glaucoma * Chronic Angle-Closure Glaucoma * Mixed mechanism glaucoma * Steroid-induced Glaucoma * Neovascular Glaucoma

Exclusion criteria

* to be less than 18 years old * to be unable to observe the study protocol * to present some risk factors for thromboembolic events and cerebrovascular accidents : hypertension, dyslipidemia, coronary artery diseases * a history of thromboembolic events and cerebrovascular accidents * congenital glaucoma * uveitic glaucoma * to be pregnant * to be breastfeeding * surgical complications prior to injection of the study drug such as vitreous in the anterior chamber or the presence of suprachoroidal hemorrhages * to have undergone a previous conjunctival surgery * to be hypersensitive to the drug, to one of the components of the drug or to one of the components of the packaging * to present an active or suspected intraocular or periocular inflammation * to have a kidney failure * to have a liver failure

Design outcomes

Primary

MeasureTime frameDescription
Failure rates of the surgery as defined by intraocular pressure reductionsone yearComplete success: post-operative IOP between 5-18 mm Hg and at least a 20% reduction in IOP from baseline without the use of glaucoma medications. Qualified success: similar definition with the use of glaucoma medications.

Secondary

MeasureTime frame
Bleb morphology using Moorfields bleb grading systemone year

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026