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To study effect of bevacizumab eye drops in patients of dry eye disease

Efficacy of topical Bevacizumab 0.05% eye drops in patients with dry eye disease - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087577
Enrollment
136
Registered
2025-05-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: H00-H05- Disorders of eyelid, lacrimal system and orbit

Interventions

Intervention1: Topical bevacizumab eye drops: Topical bevacizumab 0.05% eye drops in patients with dry eye disease Control Intervention1: standard treatment for dry eye disease: group not taking bevac

Sponsors

Dr Ankur Mishra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All patients of dry eye disease 2.Chronic symptoms of burning or foreign body sensation or itching of both eyes for 12 months

Exclusion criteria

Exclusion criteria: 1.Any structural abnormalities such as eyelid trichiasis entropion and scarring 2.Use of any other topical medication other than artificial tears within the past month 3.Use of any systemic anti inflammatory drugs or medication that may interfere with tear production such as antianxiety antidepressive and antihistamine medications within 3 months 4.A history of any Bevacizumab contraindications such as heart failure gastrointestinal perforation and pregnancy.

Design outcomes

Primary

MeasureTime frame
1.To determine the effect of topical Bevacizumab 0.05% eye drops in patients with dry eye disease 2.To compare the outcome of topical Bevacizumab 0.05% eye drops with standard care in terms of Schirmer TBUT OSDI score.Timepoint: 12 weeks duration

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Ankur Mishra

Shyam shah medical college rewa

tirkeyeva652@gmail.com9300404990

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026