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To Evaluate the Effect of Ginkgo Biloba Extract on Optic Nerve Head Perfusion Examined Using OCTA (GBE)

Primary Purpose

Glaucoma

Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Ginkgo biloba extract
Sponsored by
Nova Scotia Health Authority
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glaucoma focused on measuring Ginkgo biloba extract, Ocular perfusion, Optical coherence tomography angiography

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18 years of age or older
  • Early open angle glaucoma based on gonioscopy, clinical assessment of optic nerve head, OCT optic nerve and Humphrey Visual Field 24-2 (MD < -10dB) and positive Glaucoma Hemifield Test
  • BCVA equal or better than 6/12
  • Written consent
  • Ability to comply with treatment intervention for duration of study

Exclusion Criteria:

  • Younger than 18 years of age
  • Angle closure glaucoma or secondary open angle glaucoma
  • Refraction exceeding 6D spherical equivalent or 3D astigmatism
  • Severe corneal, lens, vitreous media opacity limit signal strength of OCTA imaging
  • Severe open angle glaucoma with visual field mean deviation worse than -10dB
  • Inability to comply to treatment intervention (e.g. swallowing difficulty)
  • History of ocular disease affecting ocular perfusion (e.g. CRAO, CRVO, diabetic retinopathy, ocular ischemic syndrome, ischemic optic neuropathy)
  • History of glaucoma surgery
  • Those taking anticoagulant therapy
  • Those with blood disorders or diabetes
  • Women who were pregnant, planning to become pregnant, or who were breast-feeding,
  • Patients with a history of seizures or who were currently taking anti-convulsant medication, and
  • Taking any drugs that may interact with GBE

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Ginkgo biloba extract group

    Arm Description

    Group receiving ginkgo biloba extract supplementation

    Outcomes

    Primary Outcome Measures

    Optic nerve head and macula perfusion
    Optic nerve head and macula perfusion will be analyzed using optical coherence tomography angiography after 4 months of ginkgo biloba extract supplementation

    Secondary Outcome Measures

    Full Information

    First Posted
    April 12, 2021
    Last Updated
    April 12, 2021
    Sponsor
    Nova Scotia Health Authority
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04846179
    Brief Title
    To Evaluate the Effect of Ginkgo Biloba Extract on Optic Nerve Head Perfusion Examined Using OCTA
    Acronym
    GBE
    Official Title
    To Evaluate the Effect of Ginkgo Biloba Extract on Optic Nerve Head Perfusion
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    May 2021 (Anticipated)
    Primary Completion Date
    May 2022 (Anticipated)
    Study Completion Date
    September 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Nova Scotia Health Authority

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Glaucoma is defined as progressive neuropathy of the optic nerve. It is an important cause of irreversible blindness worldwide. Lowering the intraocular pressure is the only proven treatment for this neurodegenerative disease. However, there is ongoing research looking at another modifiable risk factor that affects the development and progression of this disease. Ginkgo biloba (Ginkgoacease) is a tree species that has been used in traditional medicine for several hundred years to treat various diseases include improving vascular perfusion. We propose a study examining the effect of Ginkgo biloba extract supplementation on ocular perfusion using optical coherence tomography angiography.
    Detailed Description
    Glaucoma is defined as progressive neuropathy of the optic nerve. It is an important cause of irreversible blindness worldwide. Lowering the intraocular pressure is the only proven treatment for this neurodegenerative disease. However, there is ongoing research looking at another modifiable risk factor that affects the development and progression of this disease. There is growing evidence that vascular dysfunction plays a role in the pathogenesis of glaucoma. Low ocular perfusion pressure (OPP), which is expressed as the difference between mean arterial pressure and intraocular pressure (IOP), has been hypothesized to lead to glaucomatous optic neuropathy via ischemic damage to the optic nerve. The Barbados Eye Study showed that reduced OPP at baseline was associated with a three-fold increased risk of glaucoma development. Evidence has also shown that optic nerve hypoperfusion may contribute to the progression of glaucoma. Ginkgo biloba (Ginkgoacease) is a tree species that has been used in traditional medicine for several hundred years to treat various diseases. There have been recent studies that have examined its medicinal properties in treating age-related cognitive disease and neuronal degeneration resulting from ischaemic events. Studies examining systemic vascular ischemic diseases have shown a beneficial effect of ginkgo Biloba extract (GBE) on systemic arterial occlusive diseases. There is also preliminary research examining the effect GBE has on optic nerve head perfusion in patients with glaucoma. There is a study that examined the effects of antioxidants including GBE on ocular blood flow in patients with glaucoma using doppler ultrasound. When compared with patients receiving placebo, patients after antioxidant therapy containing GBE were shown to have increased peak systolic and/or end-diastolic blood velocities in all retrobulbar blood vessels, reduced vascular resistance in the central retinal and nasal short posterior ciliary arteries, increased superior and inferior temporal retinal capillary mean blood flow, an increased ratio of active to nonactive retinal capillaries. In the area of optic nerve head perfusion studies, fluorescein angiography has also been used in investigating alteration in blood flow in glaucomatous versus normal eyes. However, utility in clinical practice is limited by the qualitative nature of the test and the risk for adverse events. While color Doppler ultrasound is greatly limited in terms of resolution and can be openly used to examine large vessels of the eye. New development in ocular imaging has shown that OCTA can provide reproducible and quantifiable information about the microvasculature of the optic nerve and peripapillary retina in patients with glaucoma and can do so in a rapid and non-invasive manner avoiding some of the limitations on doppler ultrasound and fluorescein angiography. GBE Egb761 is a standardized GBE that's used in most published research on the effect of ginkgo Biloba. It is a standardized GBE used in evidence-based medicine and clinical investigations ensuring clinical standardization and a safe manufacturing process. It has much of the toxic ginkgolic acid removed leaving behind the active components of flavonoid glycosides and terpene lactones. In general, GBE is well tolerated with a low side effect profile. Several systematic reviews on research using GBE (daily dose of up to 600 mg) report no statistical difference in side effects with GBE compared with placebo. There have been some concerns regarding the bleeding risk while on ginkgo supplementation. However, randomized placebo-controlled studies in healthy volunteers have not shown any changes in bleeding time, coagulation parameters, or platelet function. Multiple studies have reported minimal adverse effects (AEs) of GBE within a specific prescribed dosage range. Overall, GBE continues to be a well-tolerated supplement with a low side effect profile. Systematic reviews of the Cochrane databases, PubMed/MEDLINE, EMBASE, and Google Scholar, report no statistically significant difference in AEs between 80 and 600 mg of GBE and placebo.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Glaucoma
    Keywords
    Ginkgo biloba extract, Ocular perfusion, Optical coherence tomography angiography

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    15 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Ginkgo biloba extract group
    Arm Type
    Experimental
    Arm Description
    Group receiving ginkgo biloba extract supplementation
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Ginkgo biloba extract
    Intervention Description
    Patients recruited to Ginkgo Biloba Extract (GBE) group will be advised to take Webber Natural Ginkgo Biloba 120 mg soft gel, 1 tablet twice a day for 4 months.
    Primary Outcome Measure Information:
    Title
    Optic nerve head and macula perfusion
    Description
    Optic nerve head and macula perfusion will be analyzed using optical coherence tomography angiography after 4 months of ginkgo biloba extract supplementation
    Time Frame
    4 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: 18 years of age or older Early open angle glaucoma based on gonioscopy, clinical assessment of optic nerve head, OCT optic nerve and Humphrey Visual Field 24-2 (MD < -10dB) and positive Glaucoma Hemifield Test BCVA equal or better than 6/12 Written consent Ability to comply with treatment intervention for duration of study Exclusion Criteria: Younger than 18 years of age Angle closure glaucoma or secondary open angle glaucoma Refraction exceeding 6D spherical equivalent or 3D astigmatism Severe corneal, lens, vitreous media opacity limit signal strength of OCTA imaging Severe open angle glaucoma with visual field mean deviation worse than -10dB Inability to comply to treatment intervention (e.g. swallowing difficulty) History of ocular disease affecting ocular perfusion (e.g. CRAO, CRVO, diabetic retinopathy, ocular ischemic syndrome, ischemic optic neuropathy) History of glaucoma surgery Those taking anticoagulant therapy Those with blood disorders or diabetes Women who were pregnant, planning to become pregnant, or who were breast-feeding, Patients with a history of seizures or who were currently taking anti-convulsant medication, and Taking any drugs that may interact with GBE

    12. IPD Sharing Statement

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    To Evaluate the Effect of Ginkgo Biloba Extract on Optic Nerve Head Perfusion Examined Using OCTA

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