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NCT Number: NCT03648814

Intracameral Versus Intravitreal Bevacizumab Injection in NVG: RCT

To prospect studying the efficacy and safety of treating NVG with the intracameral versus the intravitreal injection of Bevacizumab.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Glaucoma unit , Department of Ophthalmology Faculty of Medicine Prince of Songkla University

Hat Yai, Changwat Songkhla, 90110, Thailand

Location status: Recruiting

Location contact

WEERAWAT KIDDEE, MD

CONTACT

[email protected]

66-81271-0644

About this study

The present study comparing the safety and efficacy of 1.25mg/0.05mL Bevacizumab injection via the intracameral route versus the intravitreal route in treating the neovascular glaucoma

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of neovascular glaucoma
  • The patients having IOP > 21 mmHg, having the indication for trabeculectomy
  • The patients' age of at least 18-year-old
  • The patients having visual potential at least hand motion.
  • Present of NVI or NVA.
  • Willing and able to provide informed consent to participate in the study
  • Able to understand the purpose of the study, his/her role, and is available to return to the clinic/hospital for all required follow-up visits

Exclusion criteria

  • One eye patient
  • Patients having severe corneal edema or total hyphema obscure NVI or NVA view.
  • Cannot obtain endothelial cell count.
  • History of bevacizumab or fluorescence dye allergy.
  • Active infectious ocular disease including endophthalmitis and corneal ulcer
  • History of systemic disease including ischemic heart disease, cerebrovascular disease, end-stage renal disease, liver failure, uncontrolled hypertension
  • Has or planning to be pregnant or breastfeeding

Treatment and study plan

Intracameral injection

Procedure

A/C injection of 1.25 mg/0.05 mL bevacizumab

intravitreal injection

Procedure

Vitreous injection of 1.25 mg/0.05 mL bevacizumab

Primary outcomes

  1. regression of nevolascularization

    Time frame: 2 months

    Amount of nevolascular of iris and angle regression

Secondary outcomes

  1. IOP reduction

    Time frame: 2 months

    IOP reduction at 2-month visit compare to baseline

  2. Injection complication

    Time frame: 2 days

    Hyphema, IOP spike

Study contacts

Contact information is provided by the study sponsor or research team.

Assoc.Prof.Weerawat Kiddee, MD

CONTACT

[email protected]

+66874954626

Sponsors and collaborators

Lead sponsor

Prince of Songkla University

Other

Registry information

Official study title

Efficacy and Safety of Intracameral Versus Intravitreal Bevacizumab Injection as an Adjunctive Therapy Before Trabeculectomy With Mitomycin-C in Neovascular Glaucoma: A Prospective Randomized Trial

Important dates

Study start
2018
Primary completion
2026
Study completion
2026
First posted
Aug 27, 2018
Registry last updated
Aug 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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