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Comparison of Subconjuctival Versus Topical Bevacizumab as Adjunct Therapy to Trabeculectomy

Clinical Trial Comparing Subconjunctival and Topical Bevacizumab as Adjuncts to Trabeculectomy in Improving Outcomes for Primary Open Angle Glaucoma

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01425112
Enrollment
180
Registered
2011-08-29
Start date
2007-12-31
Completion date
2011-06-30
Last updated
2011-08-29

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

Conditions

Complications of Treatment, Progression

Keywords

trabeculectomy, bevacizumab, anti-VEGF, Efficacy

Brief summary

Bevacizumab is an anti vascular endothelial growth factor(anti-VEGF) substance that is known to reduce neovascularization and fibrovascular proliferation in inflammatory conditions, including post-operative inflammation. It has shown efficacy in numerous ocular conditions(off-label), that includes Age related macular degeneration, proliferative diabetic retinopathy, neovascular glaucoma and corneal neovascularization. It is being explored as an option for preventing recurrence of pterygium and as an adjunct to improving outcomes of trabeculectomy. There is a debate as to the mode and duration of bevacizumab administration for trabeculectomy. This study aims to compare a single subconjunctival dose of bevacizumab with topical therapy over one month in terms of outcomes of trabeculectomy surgery, non-progression of field loss and stable intraocular pressure(IOP) control.

Interventions

PROCEDUREPhacoemulsification

Surgery for complications of trabeculectomy

Sponsors

Sudhalkar Eye Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
42 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Primary Open Angle Glaucoma * Progression * Failure to reach target IOP * Non compliant

Exclusion criteria

* Resurgery * Systemic contraindication to bevacizumab * All other forms of glaucoma

Design outcomes

Primary

MeasureTime frame
Intraocular pressure controlFor 2 years

Secondary

MeasureTime frame
Progression2 years

Outcome results

None listed

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