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Intralesional Bevacizumab Injection on Primary Pterygium

A Randomized Controlled Trial of Intralesional Bevacizumab Injection on Primary Pterygium: Preliminary Results

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01380678
Acronym
bevacizumab
Enrollment
206
Registered
2011-06-27
Start date
2009-01-31
Completion date
2012-12-31
Last updated
2011-07-11

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

Conditions

Inflammation, Pterygium

Keywords

bevacizumab, pterygium, treatment, elevation

Brief summary

The purpose of this study is to evaluate that intralesional injection of bevacizumab on primary pterygium can reduce the corneal pterygium area, inflammation, redness and other symptoms.

Detailed description

To evaluate the efficacy and safety of intralesional injection of bevacizumab on primary pterygium treatment

Interventions

DRUGIntralesional injection of bevacizumab

single dose of 2 mg of bevacizumab intralesional injection on pterygium Combination of topical antazoline and tetrahydrozoline four times a day

DRUGTopical antihistamine and vasoconstrictor

combination of topical antazoline HCl 0.05% and tetrahydrozoline HCl 0.04%

Sponsors

Khon Kaen University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* primary pterygium

Exclusion criteria

* previous ocular surgery

Design outcomes

Primary

MeasureTime frameDescription
percentage of corneal pterygium area3 yearsPrior to receive the treatments, patients were asked to evaluate grading of their own symptoms and underwent clinical grading of the elevation and inflammation of the lesions using slit lamp biomicroscopy by an opthalmologist (OE). Digital photographs of each eye with pterygium were obtained for corneal pterygium area analysis \[Sony Mavica digital still camera MVC-FD83, Japan\]. Each patient was randomly assigned into either treatment group or control group using computer-generated random numbers table. Number of patients with adverse events will be recorded.

Countries

Thailand

Contacts

Primary ContactOlan Suwan-apichon, MD
osuwanapichon@hotmail.com+66 43 348383

Outcome results

None listed

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