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Effect of BGG on Glucose Metabolism and Other Markers of Metabolic Syndrome (Glucogold)

Primary Purpose

Pre Diabetes

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
BGG
Placebo
Sponsored by
Vedic Lifesciences Pvt. Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pre Diabetes focused on measuring HbA1c, Pre Diabetes, Berberine

Eligibility Criteria

20 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Able and willing to provide informed consent.
  • Treatment naïve male-female aged 20-60 years of age.
  • BMI ≥ 25 kg/m²
  • Oral glucose tolerance test (OGTT) ≥140 and ≤250 mg/dl (pre-diabetes and early diagnosed diabetes within 45 days of diagnosis)
  • Patient with chronic stable illness can be included ONLY IF he/she is currently NOT on any of the medications included in prohibited list of medicines.
  • Currently on herbal supplements can be included after a wash-out period of 7 days.
  • Subjects willing to abstain from nicotine and alcohol in the duration of the study.

Exclusion Criteria:

  • Subjects with OGTT<140 mg/dl or ≥ 250 mg/dl
  • Current treatment with diabetes medications, including metformin
  • Current treatment with glucocorticoids
  • History of clinically significant hematological, hepatic or renal diseases, as per investigator discretion
  • Uncontrolled chronic disease
  • Hormonal Disorders
  • Subjects on Steroids
  • Subjects on Statins
  • Chronic inflammatory diseases requiring any medication
  • Migraine, Sinusitis
  • Subjects Consuming NSAIDS for long term
  • Medications include the drugs of prohibited range.
  • Pregnant and lactating females.
  • Subjects addicted to nicotine, alcohol or any other recreational drug.
  • Subjects who are planning to fast for more than 4 days/ per month during the study.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    BGG

    Placebo

    Arm Description

    Dose: 01 tablet three times daily just before all major meals (breakfast, lunch and dinner)

    Matching placebo capsules [for BGG tablet] composed of micro crystalline cellulose and added colors and odors. Dose: 01 tablet three times daily just before all major meals (breakfast, lunch and dinner)

    Outcomes

    Primary Outcome Measures

    Change in Oral Disposition Index
    Change in Glycated hemoglobin

    Secondary Outcome Measures

    Change in Fasting blood sugar
    Change in Body Mass Index

    Full Information

    First Posted
    July 6, 2016
    Last Updated
    July 12, 2016
    Sponsor
    Vedic Lifesciences Pvt. Ltd.
    Collaborators
    Healthy Directions, LLC
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02834078
    Brief Title
    Effect of BGG on Glucose Metabolism and Other Markers of Metabolic Syndrome
    Acronym
    Glucogold
    Official Title
    Effect of 'Berberine Glucogold' [BGG] on Glucose Metabolism in Individuals With Marginally Impaired Glucose Metabolism Along With Other Markers of Metabolic Syndrome
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2015 (undefined)
    Primary Completion Date
    July 2016 (Actual)
    Study Completion Date
    July 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Vedic Lifesciences Pvt. Ltd.
    Collaborators
    Healthy Directions, LLC

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    According to the International Diabetes Federation, one in every 12 individuals is a diabetic (about 8% of the world population). Major risk factors of diabetes are all the aspects of modern life which include obesity, over-weight, high-risk behavior like smoking, alcohol, multiple drug use-recreational or prescribed, environmental risk factors like inactivity and lack of exercise. However there is a window of opportunity between health and disease, which is pre-diabetes. Pre-diabetes has been defined by American Diabetes Association as Impaired Glucose Tolerance (IGT) which is 7.8 -11.0 mmol/l, Impaired Fasting Glucose Test (IFT) which is 5.6-6.9mmol/l and now added Glycosylated Hemoglobin (HbA1c) of 5.7% to 6.4%. Though there are plenty of drugs available for significantly impaired glucose metabolism (including oral hypoglycemic agents and insulin), their use in marginally impaired glucose metabolism is questionable due to risk of untoward hypoglycemia. On the other hand, herbal products like curcumin, as a single ingredient has poor bioavailability problem that restricts its use as standalone treatment. Inulin works as pre-biotic and help to maintain gut microbiota which is considered as precursor for progress of prediabetes to diabetes. However, it does not have any role in primary pathophysiology of impaired glucose metabolism, i.e. pancreatic β cell dysfunction, insulin resistance, hepatic gluconeogenesis or intestinal glucose absorption. Resveratrol and omega-3 basically work on anti-oxidant pathways. None of these popular ingredients has been studied for their role in structural and functional health of pancreatic β cells which is very important for prediction of further progress of marginally impaired glucose metabolism to significantly impaired glucose metabolism. It is an unmet need to develop a product which not only improves insulin sensitivity, but also help to preserve the structural and functional health of pancreatic β cells. It also needs to improve overall metabolic and endothelial health of the person considering the close association between impaired glucose metabolism and these parameters. The proposed supplement - "Berberine GlucoGold "- is an improved version of successfully marketed supplement - Berberine GlucoDefense. It has a balanced composition in which all the ingredients complement each other in such a way that along with the individual role in glucose metabolism it also takes care of overall bioavailability and stability of the supplement. As per the previous data on ingredients, the supplement is also expected to preserve the structural and functional health of pancreatic β cells. The ingredients are also known to have positive effect on overall metabolic and endothelial health. Thus BGG has been developed to address the unmet needs in the area of glucose metabolism and overall metabolic health.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Pre Diabetes
    Keywords
    HbA1c, Pre Diabetes, Berberine

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    126 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    BGG
    Arm Type
    Experimental
    Arm Description
    Dose: 01 tablet three times daily just before all major meals (breakfast, lunch and dinner)
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Matching placebo capsules [for BGG tablet] composed of micro crystalline cellulose and added colors and odors. Dose: 01 tablet three times daily just before all major meals (breakfast, lunch and dinner)
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    BGG
    Intervention Type
    Other
    Intervention Name(s)
    Placebo
    Primary Outcome Measure Information:
    Title
    Change in Oral Disposition Index
    Time Frame
    Day 0, Day 28, Day 56 and Day 84
    Title
    Change in Glycated hemoglobin
    Time Frame
    Day 0, Day 28, Day 56 and Day 84
    Secondary Outcome Measure Information:
    Title
    Change in Fasting blood sugar
    Time Frame
    Day 0, Day 28, Day 56 and Day 84
    Title
    Change in Body Mass Index
    Time Frame
    Day 0, Day 28, Day 56 and Day 84

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Able and willing to provide informed consent. Treatment naïve male-female aged 20-60 years of age. BMI ≥ 25 kg/m² Oral glucose tolerance test (OGTT) ≥140 and ≤250 mg/dl (pre-diabetes and early diagnosed diabetes within 45 days of diagnosis) Patient with chronic stable illness can be included ONLY IF he/she is currently NOT on any of the medications included in prohibited list of medicines. Currently on herbal supplements can be included after a wash-out period of 7 days. Subjects willing to abstain from nicotine and alcohol in the duration of the study. Exclusion Criteria: Subjects with OGTT<140 mg/dl or ≥ 250 mg/dl Current treatment with diabetes medications, including metformin Current treatment with glucocorticoids History of clinically significant hematological, hepatic or renal diseases, as per investigator discretion Uncontrolled chronic disease Hormonal Disorders Subjects on Steroids Subjects on Statins Chronic inflammatory diseases requiring any medication Migraine, Sinusitis Subjects Consuming NSAIDS for long term Medications include the drugs of prohibited range. Pregnant and lactating females. Subjects addicted to nicotine, alcohol or any other recreational drug. Subjects who are planning to fast for more than 4 days/ per month during the study.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Sandip Patil, M.D.
    Organizational Affiliation
    Maharashtra Council of Indian Medicine
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Rajesh Kewalramani, M.B.B.S.
    Organizational Affiliation
    Maharashtra Council of Indian Medicine
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Effect of BGG on Glucose Metabolism and Other Markers of Metabolic Syndrome

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