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Efficacy of subconjunctival bevacizumab injections before and after surgical excision in preventing pterygium recurrence

Evaluating postoperative pterygium recurrence rate modifications in patients receiving subconjunctival bevacizumab injections before and after surgical excision with bare sclera technique

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11424742
Enrollment
80
Registered
2017-04-18
Start date
2015-12-01
Completion date
Unknown
Last updated
2017-07-24

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

Conditions

Pterygium Eye Diseases Pterygium

Interventions

Participants will be randomized to one of the following groups: Study group: Subconjunctival injection of Bevacizumab (2.5 mg/0.1 ml) followed by pterygium surgical excision with bare sclera techniqu

Sponsors

S. Luigi Gonzaga University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged over 18 years 2. Pterygium in one/both eye(s) extending more than 1 mm across the limbus

Exclusion criteria

Exclusion criteria: 1. Pregnancy 2. Ocular surface disease or infection 3. Autoimmune disorders 4. Previous limbal or corneal surgery

Design outcomes

Primary

MeasureTime frame
Recurrence of pterygium (defined by growth of fibrovascular tissue extending more than 1 mm across the limbus), assessed by ophthalmological examination during follow-up visits at 1 week, 1 month, 3 and 6 months after the second subconjunctival injection (for the study group) or after surgery (for the control group).

Secondary

MeasureTime frame
1. Grading of pterygium vascularization (according to the scheme proposed by Tan et al., Arch Ophthalmol 1997), assessed by ophthalmological examination during follow-up visits at 1 day, 1 month, 3 and 6 months after the second subconjunctival injection (for the study group) or after surgery (for the control group) 2. Pterygium dimensions, assessed by comparison of ocular anterior segment photographs captured 1 week before treatment with pictures captured at 1 week, 1 month 3 and 6 months follow-up visits

Countries

Italy

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 27, 2026