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Completed

NCT Number: NCT03154892

The Effect of Conbercept Injection Through Different Routes for Neovascular Glaucoma

The neovascular glaucoma (NVG) is a refractory type of secondary glaucoma and often lead to frustrated treatment and blindness. It has been confirmed high levels of vascular endothelial growth factor (VEGF) in NVG. Conbercept is an anti-VEGF agent,its role in regression of other neovascular disorders such as wet-type age-related macular degeneration and diabetic retinopathy has been described. Investigators aim to evaluate the efficacy and safety of intracameral and intravitreal injection of conbercept for the treatment of NVG.

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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Ophthalmology, Second affiliated hospital of Xian Jiaotong University

Xi'an, Shaanxi, 710004, China

About this study

The neovascular glaucoma (NVG) is a refractory type of secondary glaucoma and often lead to frustrated treatment and blindness. It has been confirmed high levels of vascular endothelial growth factor (VEGF) in NVG. Conbercept is an anti-VEGF agent,Its role in regression of other neovascular disorders such as wet-type age-related macular degeneration and diabetic retinopathy has been described. The intravitreal injection of anti-VEGF agent has shown its therapeutic potential for the early stage of NVG, but not for the late stage. Intracameral injection maybe used as an alternative way for administration. Investigators aim to evaluate the efficacy and safety of intracameral and intravitreal injection of conbercept for the treatment of NVG.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with a diagnosis of neovascular glaucoma (Stage 1-2-3)
  • Individuals who are ages 20-80 years old; male or female of chinese
  • Visual acuity of light perception or better in the study eye
  • Willing and able to comply with clinic visits and study-related procedures
  • Provide signed informed consent

Exclusion criteria

  • Use of intraocular anti-VEGF agents in the study eye in the past 3 months.
  • Active ocular or periocular infection in the study eye
  • Uncontrolled Blood Pressure
  • Thromboembolism
  • Congestive Heart Failure
  • Renal Failure
  • History of myocardial infarction
  • History of Stroke
  • Pregnant or breast-feeding women
  • Participation in another simultaneous medical investigator or trial

Treatment and study plan

Intracameral injection

Procedure

Intracameral Conbercept injection for the treatment of NVG

intravitreal injection

Procedure

Intravitreal Conbercept injection for the treatment of NVG

Primary outcomes

  1. NVI/NVA

    Time frame: 1 week and 1 month after operation

    Changes in extent of iris or angle neovascularization

Secondary outcomes

  1. IOP

    Time frame: 1 week and 1 month after operation

    Changes in Intraocular pressure

  2. BCVA

    Time frame: 1 week and 1 month after operation

    Changes in best corrected visual acuity

Sponsors and collaborators

Lead sponsor

Second Affiliated Hospital of Xi'an Jiaotong University

Other

Registry information

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
May 16, 2017
Registry last updated
May 23, 2018

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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