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Assessing Combined Bevacizumab-Mitomycin C Use During Ahmed Valve Revision in Recurrent Pediatric Glaucoma

Evaluation of Combined Bevacizumab-Mitomycin C Use During Ahmed Valve Revision in Recurrent Pediatric Glaucoma

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06983704
Acronym
MMC glaucoma
Enrollment
50
Registered
2025-05-21
Start date
2024-02-09
Completion date
2025-02-15
Last updated
2025-05-21

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

Conditions

Pediatric Glaucoma

Keywords

Pediatric glaucoma, Ahmed valve, bevacizumab, mitomycin C

Brief summary

To asess the efficacy and safety of combining subconjunctival bevacizumab with mitomycin C (MMC) during AGV revision surgery in pediatric patients with recurrent glaucoma.

Detailed description

Recurrent pediatric glaucoma following Ahmed Glaucoma Valve (AGV) implantation presents a therapeutic challenge. This study evaluates the efficacy and safety of combining subconjunctival bevacizumab with mitomycin C (MMC) during AGV revision surgery in pediatric patients with recurrent glaucoma.

Interventions

PROCEDUREAGV plate

AGV plate using a 27-gauge needle

PROCEDUREbevacizumab injection

subconjunctival injection of bevacizumab

Sponsors

Benha University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
No minimum to 12 Years
Healthy volunteers
No

Inclusion criteria

* children under 12 years with previous AGV implantation for primary congenital glaucoma

Exclusion criteria

* age \>12 years, eyes with no light perception, and those with prior cyclodestructive procedures.

Design outcomes

Primary

MeasureTime frameDescription
surgical successfor 12 monthsIOP ≤ 21 mmHg and ≥ 5 mmHg without medications

Countries

Egypt

Outcome results

None listed

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