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
About this trial
This is an interventional treatment trial for Pre Diabetes focused on measuring HbA1c, Pre Diabetes, Berberine
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.
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
NCT ID
NCT02834078
First Posted
July 6, 2016
Last Updated
July 12, 2016
Sponsor
Vedic Lifesciences Pvt. Ltd.
Collaborators
Healthy Directions, LLC
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
Learn more about this trial
Effect of BGG on Glucose Metabolism and Other Markers of Metabolic Syndrome
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