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Safety and efficacy of subconjunctival bevacizumab compared with placebo in the management of acquired cornea opacity with neovascularization.

Safety and efficacy of subconjunctival bevacizumab compared with placebo in the management of acquired cornea opacity with neovascularization.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
PACTR
Registry ID
PACTR202509763211872
Enrollment
64
Registered
2025-09-11
Start date
2025-10-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Eye Diseases

Interventions

Sponsors

Abe Adeola
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who give their consents. 2. Patients with grade 2 and 3 corneal opacity, with associated neovascularization grade 2 to 4 who present to the eye clinic of LASUTH within the period of study. 3. Age-18 years ( legal age for consent in Nigeria ) to 80 years. 4. Patients not on any anti VEGF therapy in the previous one month.

Exclusion criteria

Exclusion criteria: 1. Patients younger than 18yrs. 2. Patients with an active ocular inflammation or infection. 3. Patients with visual impairment from other causes like cataract, uncontrolled glaucoma and macular disorders. 4. Patient with no light perception in the eye for study. 5. Patient with an only eye. 6. Patients with an uncontrolled hypertension and other contraindications to bevacizumab like cardiac diseases, renal failure and gastrointestinal perforations. 7. Pregnant and lactating mothers.

Design outcomes

Primary

MeasureTime frame
The primary outcome measures will be: 1.The number of corneal surface segment covered by opacity using digital pictures with a specially made computer-generated pattern of segments which is to be fitted over the digital corneal photograph taken for the estimation. And 2. The number of corneal surface segments with corneal neovascularization.

Secondary

MeasureTime frame
Secondary outcome measures will be: 1.The best corrected visual acuity. 2.complications related to the interventions and 3.participants’ quality of life changes.

Countries

Nigeria

Contacts

Public ContactSedoten Bashorun

Consultant Department of Ophthalmology LASUTH

sedoten_12@yahoo.com+23423688141

Outcome results

None listed

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