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Strategies for Management of Corneal Neovascularisation

Primary Purpose

Corneal Neovascularisation

Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Fine Needle Diathermy
Bevacizumab
Sponsored by
University of Nottingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Corneal Neovascularisation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients over the age of 18
  • Able to give informed consent
  • With corneal neovascularisation non responsive or not suitable for conventional steroid therapy
  • Use of effective contraception in females of childbearing age

Exclusion Criteria:

  • Patients under 18 years of age
  • Patients unable or refusing to provide informed consent
  • Patients who are needle phobic
  • Pregnant women, women aiming for conception and breastfeeding women
  • Patients with hypersensitivity to the active substance or to any of the excipients
  • Patients with active or suspected ocular or periocular infections.
  • Patients with active severe intraocular inflammation.
  • Patients with raised intraocular pressure or on glaucoma medication

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Fine needle Diathermy

    Fine Needle Diathermy and Bevacizumab

    Arm Description

    Fine needle Diathermy(FND) will be applied under topical anaesthesia under an operating microscope. This involves the insertion of a fine corneal suture needle in the vicinity of the vessels and using this as an extension of the probe of a monopolar cautery to deliver the energy in the corneal tissue at the site at which it is required to occlude the vessels.

    Fine needle Diathermy(FND) will be applied under topical anaesthesia under an operating microscope. This involves the insertion of a fine corneal suture needle in the vicinity of the vessels and using this as an extension of the probe of a monopolar cautery to deliver the energy in the corneal tissue at the site at which it is required to occlude the vessels. Patients will receive subconjunctival injections of bevacizumab in the conjunctiva near the limbus in the quadrant(s) affected (total volume of between 0.2 ml-0.3 ml of the 2.5 mg/0.1 ml solution). The subconjunctival injections will be administered after FND in the same treated quadrants.

    Outcomes

    Primary Outcome Measures

    Decreased corneal neovascularisation
    A comparison of total vascularisation of the corneal area as measured by our grading system (Faraj LA et al, 2015) before and after treatment.

    Secondary Outcome Measures

    Improved/maintained Snellen's visual acuity
    Visual acuity is assessed using Snellen chart and vision is expressed in LOGMAR units
    Decreased corneal opacity related to lipid deposition
    The response to treatment will be judged clinically by biomicroscopy examination and quantitatively by comparison with pre-treatment slit lamp photographs. The comparison of the pre and post treatment slit lamp images will be done by two independent blind reviewers.
    Reduced episodes of graft rejection(in corneal graft patients)
    Number of rejection episodes will be recorded

    Full Information

    First Posted
    October 27, 2015
    Last Updated
    December 1, 2015
    Sponsor
    University of Nottingham
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02594423
    Brief Title
    Strategies for Management of Corneal Neovascularisation
    Official Title
    Management of Active and Established Corneal Neovascularisation to Prevent Visual Impairment
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2015
    Overall Recruitment Status
    Unknown status
    Study Start Date
    December 2015 (undefined)
    Primary Completion Date
    August 2017 (Anticipated)
    Study Completion Date
    August 2018 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Nottingham

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The cornea is the transparent window of the eye, which allows light to enter into the eye and also contributes to the focusing of the light rays. One of the major factors responsible for its transparency is the lack of blood vessels. However, following inflammation new blood vessels (corneal vascularisation [CVas]) grow into the cornea affecting its transparency and impairing vision. CVas leads to further damage in the form of scarring,oedema,fat deposition and is a major cause of corneal graft rejection. In 2000 with ethical approval (OY129801) the investigators developed and published a clinical technique called Fine Needle Diathermy occlusion of corneal vessels (FND). This has proven very successful for occluding established vessels and is practiced in many centers across the world. Recently it has been demonstrated that by inhibiting a chemical stimulant of vessel formation called vascular endothelial growth factor(VEGF) active new vessel growth in the retina can be suppressed. The approach is also being used for corneal new vessels. Bevacizumab (Avastin) is a chemical inhibitor of VEGF and is used extensively to treat retinal new vessels in macular degeneration. Avastin has been shown to be effective and safe in treating corneal new vessels. The investigators propose to evaluate the efficacy and safety of FND alone and FND combined with Avastin in treatment of CVas.
    Detailed Description
    Corneal neovascularisation is a very common problem affecting both sexes at all ages and induced by differing underlying causes. It is considered to be the single most important risk factor for graft rejection. The process of angiogenesis, i.e. the formation of new blood vessels, is similar in any part of the body. Hence principles adopted to alleviate new blood vessels in one area can be applied to blood vessels in other areas using similar drugs. Over the past 8 years a component necessary for angiogenesis, i.e Vascular endothelial growth factor (VEGF) has been targeted to induce regression of blood vessels in patients with cancer with an intravenous dosage of an anti-VEGF. More recently, anti-VEGF therapies have targeted eye related neovascularisation, especially in the treatment of age related macular degeneration. This role has been expanded to include all other structures in the eye affected by angiogenesis such as neovascular glaucoma(Iris) and diabetic retinopathy(Retina). Over the past few years attention has been drawn to the use of antiVEGF therapies to the surface of the eye. Many reports in international peer reviewed literature have commented on the use of anti VEGF therapy in the form of drops or injections on the surface of the eye, subconjunctivally and within the cornea. They have found drops and injections are safe, although injections appear to act more favourably. Avastin has been investigated for treating corneal new vessels and was proved to be both safe and effective. Fine needle diathermy (FND) is a routine method for occluding corneal vessels that was developed in our department in 2000 and is used worldwide. It has been established that this technique is suitable for active and mature vessels. However, the consequent transient tissue injury and inflammation can trigger further new vessel formation. Avastin is effective in occlusion of the active vessels only.It does not affect the established mature vessels. Hence if FND is combined with Avastin it is expected and hypothesized that a more efficient and lasting occlusion of vessels will be obtained. In this study, the investigators aim to investigate the combined action of Avastin and fine needle diathermy in occlusion of corneal vessels. The actual incidence of corneal neovascularisation in the UK is unknown but American studies suggest up to 1.4 million people are affected with sight threatening complications on annual basis. These blood vessels arise from a multitude of causes, including viral infections, corneal injuries, chronic inflammation and as a result of corneal transplantation. Conventional therapies at the present time include surgical occlusion of the blood vessels with a diathermy or laser or chronic use of steroids. The latter option is a associated with potential sight threatening complications such as glaucoma. This study will generate data to inform further controlled studies towards establishing Avastin and fine needle diathermy as the treatment of choice for corneal new vessels.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Corneal Neovascularisation

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    40 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Fine needle Diathermy
    Arm Type
    Active Comparator
    Arm Description
    Fine needle Diathermy(FND) will be applied under topical anaesthesia under an operating microscope. This involves the insertion of a fine corneal suture needle in the vicinity of the vessels and using this as an extension of the probe of a monopolar cautery to deliver the energy in the corneal tissue at the site at which it is required to occlude the vessels.
    Arm Title
    Fine Needle Diathermy and Bevacizumab
    Arm Type
    Active Comparator
    Arm Description
    Fine needle Diathermy(FND) will be applied under topical anaesthesia under an operating microscope. This involves the insertion of a fine corneal suture needle in the vicinity of the vessels and using this as an extension of the probe of a monopolar cautery to deliver the energy in the corneal tissue at the site at which it is required to occlude the vessels. Patients will receive subconjunctival injections of bevacizumab in the conjunctiva near the limbus in the quadrant(s) affected (total volume of between 0.2 ml-0.3 ml of the 2.5 mg/0.1 ml solution). The subconjunctival injections will be administered after FND in the same treated quadrants.
    Intervention Type
    Device
    Intervention Name(s)
    Fine Needle Diathermy
    Intervention Description
    Fine needle diathermy is a surgical procedure that is used in the treatment of corneal NV. It is a safe and effective method for corneal vessels occlusion.
    Intervention Type
    Drug
    Intervention Name(s)
    Bevacizumab
    Other Intervention Name(s)
    Avastin(BEVACIZUMAB)
    Intervention Description
    Bevacizumab is a humanized monoclonal antibody that binds to isoforms of VEGF-A .
    Primary Outcome Measure Information:
    Title
    Decreased corneal neovascularisation
    Description
    A comparison of total vascularisation of the corneal area as measured by our grading system (Faraj LA et al, 2015) before and after treatment.
    Time Frame
    6 months
    Secondary Outcome Measure Information:
    Title
    Improved/maintained Snellen's visual acuity
    Description
    Visual acuity is assessed using Snellen chart and vision is expressed in LOGMAR units
    Time Frame
    10 months
    Title
    Decreased corneal opacity related to lipid deposition
    Description
    The response to treatment will be judged clinically by biomicroscopy examination and quantitatively by comparison with pre-treatment slit lamp photographs. The comparison of the pre and post treatment slit lamp images will be done by two independent blind reviewers.
    Time Frame
    10 months
    Title
    Reduced episodes of graft rejection(in corneal graft patients)
    Description
    Number of rejection episodes will be recorded
    Time Frame
    10 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients over the age of 18 Able to give informed consent With corneal neovascularisation non responsive or not suitable for conventional steroid therapy Use of effective contraception in females of childbearing age Exclusion Criteria: Patients under 18 years of age Patients unable or refusing to provide informed consent Patients who are needle phobic Pregnant women, women aiming for conception and breastfeeding women Patients with hypersensitivity to the active substance or to any of the excipients Patients with active or suspected ocular or periocular infections. Patients with active severe intraocular inflammation. Patients with raised intraocular pressure or on glaucoma medication
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Harminder S Dua, Professor
    Phone
    +44 (0) 115970 9796
    Email
    harminder.dua@nottingham.ac.uk
    First Name & Middle Initial & Last Name or Official Title & Degree
    Noha M Ghoz, Fellow
    Phone
    +44 (0) 115 9949924
    Ext
    63735
    Email
    msxng2@nottingham.ac.uk
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Harminder S Dua, Professor
    Organizational Affiliation
    University of Nottingham
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Strategies for Management of Corneal Neovascularisation

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