Measurement of the Effect of Gingko Biloba Extract on Ocular and Nailfold Blood-flow in NTG

Sponsor
Robert Ritch, MD, LLC. (Other)
Overall Status
Unknown status
CT.gov ID
NCT03761992
Collaborator
(none)
40
1
2
24.4
1.6

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the effect of Ginkgo biloba extract (GBE) on the number of blood vessels in the back of the eye as well as the amount of blood flow at the nailfold(where the fingernail meets the skin) of the 4th finger in the hand.This finger, along with the 5th finger, has the most transparent skin, which makes imaging a little easier. GBE is an over-the-counter pill, made from a natural powder taken from the Gingko (Maidenhair) tree, that is widely used. A technique called Optical Coherence Tomography Angiography (OCTA),will be used to measure the small blood vessels at the back of the eye, the macula (the area of sharpest vision), and the optic disc (the point at which the nerve fibers from the retina enter to form the optic nerve, which transmits visual impulses to the brain).

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Gingko Baloba
  • Other: Placebo
N/A

Detailed Description

GBE has been reported to improve blood flow to the brain, eye, and extremeties(hands, feet,etc.). .As with most supplements, GBE is neither regulated nor FDA approved.

A technique called Optical Coherence Tomography Angiography (OCTA),will be used to measure the small blood vessels at the back of the eye, the macula (the area of sharpest vision), and the optic disc (the point at which the nerve fibers from the retina enter to form the optic nerve, which transmits visual impulses to the brain). This technique uses a camera, capable of imaging the smallest vessels, so that their density (number) can be calculated by a computer. This is being done to determine if there is disease causing increasing loss of these vessels. The imaging is done by a widely used camera which does not contact the eye. It simply uses visible light to measure the amount of blood vessels present in a determined area in the back of the eye. Blood flow at the 4th finger nailfold (nailfold capillaroscopy; NFC) is a standard technique, especially in rheumatology, performed by using a commercially available light microscope which glides over the base of the fingernail and can image the tiny capillaries in the nailfold. These images are recorded as videos from which the blood flow can be analyzed by freely available software for the purpose of quantitative measurements (amount of blood flow and blood flow velocity).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Gingko baloba extract (GBE) versus placeboGingko baloba extract (GBE) versus placebo
Masking:
Double (Participant, Investigator)
Masking Description:
Neither the patient nor the investigator will know which treatment that the patient is receiving.
Primary Purpose:
Treatment
Official Title:
Measurement of the Effect of Gingko Biloba Extract on Ocular and Nailfold Blood-flow in Normaltension Glaucoma by Ocular Coherence Tomography Angiography and Nailfold Capillaroscopy
Actual Study Start Date :
Nov 19, 2018
Anticipated Primary Completion Date :
Nov 1, 2020
Anticipated Study Completion Date :
Dec 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Gingko Biloba Extract

Gingko Biloba Extract 240 mg.

Dietary Supplement: Gingko Baloba
Tablets
Other Names:
  • 240mg. Gingko Biloba
  • Placebo Comparator: Placebo

    Placebo Pill

    Other: Placebo
    Tablets

    Outcome Measures

    Primary Outcome Measures

    1. Primary Outcome - Measure of Blood Vessel by Optical Cohrence Tomography Angiography (OCTA) [4 weeks]

      The investigators plan to evaluate the density of the small blood vessels at the back of the eye. This will be measured by a OCTA. A camera capable of imaging the smallest vessels so that their density (number) can be calculated by a computer, the purpose being to determine if there is disease causing progressive loss of these vessels.

    Secondary Outcome Measures

    1. Secondary Outcome - Measure of Blood Flow and Velocity by Nailfold Capillaroscopy (NFC) [4 weeks]

      Measuring blood flow at the 4th finger nailfold by NFC is a standard technique, especially in rheumatology, in which a commercially available light microscope glides over the base of the fingernail to image the tiny capillaries in the nailfold. These images are recorded as videos from which the blood flow can be analyzed quantitatively by freely available software to measure blood flow and velocity.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    Male or female of any race, at least 18 years of age

    • Has provided verbal and written informed consent.

    • Able and willing to follow instructions, including participation in all study assessments and visits.

    • Eyes with NTG will be enrolled.

    • Glaucoma severity will be graded using the WHO (World Health Organization)staging system.

    NTG diagnosis will be based on the following:
    1. Glaucomatous optic disc on slit-lamp biomicroscopy defined as cup-to-disc ratio greater than 0.7, inter-eye asymmetry in cup-to-disc ration greater than 0.2 or neuroretinal rim notching, focal thinning, disc hemorrhage or vertical elongation of optic disc.

    2. Glaucomatous visual field defects on at least three reliable visual field examinations as measured by a glaucoma hemifield test (GHT) result outside normal limits and/or the appearance of at least three consecutive test points on the pattern deviation plot with p<1% and at least one at p<0.05%, not including points on the edge of the field.

    3. NTG will be defined as those subjects with a history of untreated peak IOP ≤21 mmHg.

    • Both eyes will be enrolled
    Exclusion Criteria:
    • Best-corrected visual acuity less than 20/40

    • Age younger than 18 years or older than 85 years

    • Refractive error greater than +3.00 diopters (D) or less than -7.00 diopters (D)

    • Previous intraocular surgery except for uncomplicated cataract extraction with posterior chamber intraocular lens implantation

    • Any other diseases that may cause visual field loss or optic disc abnormalities

    • Inability to perform reliably on automated visual field testing.

    • Subjects taking any GBE product will be washed out for 2 weeks prior to enrollment.

    • Diabetes.

    • Seizure disorder.

    • Taking any drugs that may interact with GBE (as listed).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 New York Eye and Ear Infirmary of Mount Sinai New York New York United States 10003

    Sponsors and Collaborators

    • Robert Ritch, MD, LLC.

    Investigators

    • Principal Investigator: Robert Ritch, MD, New York Eye and Ear Infirmary of mount Sinai

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Robert Ritch, MD, LLC.
    ClinicalTrials.gov Identifier:
    NCT03761992
    Other Study ID Numbers:
    • NFC Gingko
    First Posted:
    Dec 3, 2018
    Last Update Posted:
    Mar 17, 2020
    Last Verified:
    Mar 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 17, 2020