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Randomized Controlled Trial of Subconjunctival Bevacizumab Injection in Impending Recurrent Pterygium

A Pilot Study of Subconjunctival Bevacizumab Injection in Impending Recurrent Pterygium

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01288404
Enrollment
80
Registered
2011-02-02
Start date
2008-01-31
Completion date
2010-11-30
Last updated
2011-02-02

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

Conditions

Pterygium of the Conjunctiva and Cornea

Keywords

Bevacizumab, impending recurrent pterygium

Brief summary

Hypothesis: Subconjunctival bevacizumab injection may potentially suppress neovascularization in pterygium, preventing or retarding the progression of recurrence.

Detailed description

1. Impending recurrent pterygium 2. Anti-VEGF therapy * Bevacizumab * Subconjunctival injection * Suppress neovascularization

Interventions

topical 0.1% fluorometholone eye drops 4 times daily for 4 weeks

DRUGBevacizumab

subconjunctival bevacizumab 1.25 mg/0.05mL

Sponsors

Ramathibodi Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

1. Impending recurrent pterygium developed within 6 months following pterygium surgery either simple excision or excision with grafting. 2. Failure of conventional topical anti-inflammatory therapy for impending recurrent pterygium which was defined by the progression of fibrovascular tissue over the excised area despite receiving treatment. 3. No history of any adjunctive treatment such as MMC, 5-FU, periocular injection of corticosteroids and beta radiation. 4. No other ocular surface pathologies or coexisting ocular diseases. 5. No other ocular surgeries within the previous 6 months. 6. No history of allergy to the medications used in this study. 7. Good compliance with the study regimen and availability for the duration of the entire study period.

Exclusion criteria

1. Platelet disorders 2. Hypertension 3. Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
Severity of impending recurrent pterygium3 months

Secondary

MeasureTime frame
Visual analog scales3 months
Adverse reactions3 months

Countries

Thailand

Outcome results

None listed

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