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Effect of Irvingia Gabonensis Administration on Metabolic Syndrome, Insulin Secretion and Insulin Sensitivity

Primary Purpose

Metabolic Syndrome X

Status
Completed
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Irvingia gabonensis
Placebo
Sponsored by
University of Guadalajara
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metabolic Syndrome X focused on measuring Metabolic Syndrome, Irvingia gabonensis, African mango, Insulin resistance

Eligibility Criteria

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

Inclusion Criteria:

  • Patients both sexes
  • Age between 30 and 60 years
  • Metabolic syndrome according IDF modified criteria
  • Waist circumference: Men ≥90 cm, women ≥80 cm

And two of the following criteria:

  • HDL-C: Men ≤40 mg/dL, women ≤50 mg/dL
  • Fasting glucose ≥100 mg/dL
  • Triglycerides ≥150 mg/dL
  • Blood pressure ≥130/85 mmHg
  • Informed consent signed

Exclusion Criteria:

  • Women with confirmed or suspected pregnancy
  • Women under lactation and/or puerperium
  • Known hypersensibility to Irvingia gabonensis
  • Physical impossibility for taking pills
  • Known uncontrolled renal, hepatic, heart or thyroid disease
  • Previous treatment for the metabolic syndrome components
  • Body mass index ≥ 39.9 kg/m2
  • Fasting glucose ≥126 mg/dL
  • Triglycerides ≥ 500 mg/dL
  • Total cholesterol ≥ 240 mg/dL
  • LDL-C ≥190 mg/dL
  • Blood pressure ≥140/90 mmHg

Sites / Locations

  • Instituto de Terapéutica Experimental y Clínica

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Irvingia gabonensis

Placebo

Arm Description

Irvingia gabonensis will be administered 150 mg before breakfast and 150 before dinner during 12 weeks

Placebo will be administered 150 mg before breakfast and 150 before dinner during 12 weeks

Outcomes

Primary Outcome Measures

Fasting Glucose Levels at Week 12
Fasting glucose will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Triglycerides Levels at Week 12
Triglycerides will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
High Density Lipoprotein (HDL-C) Levels at Week 12
The HDL-C will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Systolic Blood Pressure at Week 12
The systolic and blood pressure will be evaluated at baseline and at week 12 with a digital sphygmomanometer
Diastolic Blood Pressure at Week 12.
The diastolic and blood pressure will be evaluated at baseline and at week 12 with a digital sphygmomanometer
Waist Circumference at Week 12
The waist circumference will be evaluated at baseline and at week 12 with a flexible validated metric tape
First Phase of Insulin Secretion at Week 12
The first phase of insulin secretion will be calculated at baseline and week 12 with the stumvoll index from concentrations of glucose and insulin obtained of an oral glucose tolerance test. Human studies support the critical physiologic role of the first-phase of insulin secretion in the maintenance of postmeal glucose homeostasis. First phase of insulin secretion was estimated using the Stumvoll index (1283+ 1.829 x insulin 30' - 138.7 x glucose 30' + 3.772 x insulin 0'), the entered values reflect the first phase of insulin secretion
Total Insulin Secretion at Week 12
Total insulin secretion will be calculated at baseline and week 12 with the insulinogenic index from concentrations of glucose and insulin obtained of an oral glucose tolerance test. The insulinogenic index is a ratio that relates enhancement of circulating insulin to the magnitude of the corresponding glycemic stimulus. Total insulin secretion was calculated with the insulinogenic index (ΔABC insulin/ΔABC glucose), the entered values reflect the total insulin secretion
Total Insulin Sensitivity at Week 12
Insulin sensitivity will be calculated at baseline and week 12 with the stumvoll index from concentrations of glucose and insulin obtained of an oral glucose tolerance test. Matsuda Index value is used to indicate insulin resistance on diabetes. Insulin sensitivity was calculated with Matsuda index [10,000 / √glucose 0' x insulin 0') (mean glucose oral glucose tolerance test (OGTT) x mean insulin OGTT)]. The entered values reflect the insulin sensitivity

Secondary Outcome Measures

Body Weight at Week 12
The body weight will be measured at baseline and week 12 with a bioimpedance balance.
Body Mass Index at Week 12
The body mass index will be calculated at baseline and week 12 with the Quetelet index
Total Cholesterol at Week 12
Total cholesterol will be estimated bye standardized techniques at baseline and week 12
Low Density Lipoproteins (LDL-C) at Week 12
The LDL-C will be calculated at baseline and week 12 with the Friedewald formula
Aspartate Aminotransferase at Week 12
The aspartate aminotransferase will be determinated by standardized techniques at baseline and week 12
Alanine Aminotransferase at Week 12
The alanine aminotransferase will be determinated by standardized techniques at baseline and week 12
Creatinine at Week 12
Creatinine levels will be measured at baseline and week 12 with standardized techniques
Uric Acid at Week 12
Uric acid levels will be measured at baseline and week 12 with standardized techniques

Full Information

First Posted
January 29, 2015
Last Updated
September 11, 2020
Sponsor
University of Guadalajara
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1. Study Identification

Unique Protocol Identification Number
NCT02354339
Brief Title
Effect of Irvingia Gabonensis Administration on Metabolic Syndrome, Insulin Secretion and Insulin Sensitivity
Official Title
Effect of Irvingia Gabonensis Administration on Metabolic Syndrome, Insulin Secretion and Insulin Sensitivity
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
January 2015 (Actual)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Guadalajara

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The metabolic syndrome is a high prevalence disease worldwide. About a quarter of the adult population suffers from the disease and predispose the onset of diseases like cardiovascular disease and diabetes mellitus type 2. The first line of treatment for metabolic syndrome is diet and exercise but patients have a low attachment to the treatment, so pharmacologic therapy is required. There is no a single drug that could help to the treatment of all metabolic syndrome components. Irvingia gabonensis, better known as African mango, is widely consumed in central and western Africa, mainly the fruit and seeds. Besides being part of the diet of African the seeds have been used for the treatment of diseases such as dysentery, diabetes and as an analgesic. Resent investigations have demonstrated that an extract of African mango seeds induce significantly weight loss in subjects with obesity, and also improves some biochemical parameters such as glucose and the lipid profile. The aim of this study is to evaluate the effect of Irvingia gabonensis on metabolic syndrome, insulin secretion and insulin sensitivity.
Detailed Description
A randomized, double-blind, placebo-controlled, clinical trial is going to be carried out in 24 patients of both sexes aged between 30 and 60 years, with diagnosis of metabolic syndrome according to the modified International Diabetes Federation (IDF) criteria (without diabetes and without previous treatment for metabolic syndrome components). The patients will be assigned randomly into two groups of 12 patients each. The patients will receive 150 mg of Irvingia gabonensis before breakfast and dinner (300 mg per day) or placebo during 12 weeks. Waist circumference, triglycerides, high density lipoproteins (HDL-c) and blood pressure will be evaluated before and after intervention in both groups. First phase of insulin secretion (Stumvoll index), total insulin secretion (Insulinogenic index) and Insulin sensitivity (Matsuda index) will be calculated from the concentration of glucose and insulin obtained from an Oral Glucose Tolerance Test. Data from statistical analysis will be presented through measures of central tendency and dispersion, mean and standard deviation for quantitative variables and frequencies and percentages for qualitative variables. Qualitative variables will be analyzed by X2. The inter group differences will be analyzed through Mann-Whitney U test and Wilcoxon Test for intra-group differences. Statistical significance will be considered with a p<0.05. This protocol was approved by a local ethics committee and written informed consent will be obtained from all volunteers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome X
Keywords
Metabolic Syndrome, Irvingia gabonensis, African mango, Insulin resistance

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a study with two groups of patients with metabolic syndrome. One group received Irvingia Gabonensis and the other received placebo as control.
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Irvingia gabonensis
Arm Type
Experimental
Arm Description
Irvingia gabonensis will be administered 150 mg before breakfast and 150 before dinner during 12 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo will be administered 150 mg before breakfast and 150 before dinner during 12 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
Irvingia gabonensis
Other Intervention Name(s)
African mango
Intervention Description
Intervention will be administered 30 minutes before meals
Intervention Type
Other
Intervention Name(s)
Placebo
Other Intervention Name(s)
calcined magnesia
Intervention Description
Intervention will be administered 30 minutes before meals
Primary Outcome Measure Information:
Title
Fasting Glucose Levels at Week 12
Description
Fasting glucose will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Time Frame
12 weeks
Title
Triglycerides Levels at Week 12
Description
Triglycerides will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Time Frame
12 weeks
Title
High Density Lipoprotein (HDL-C) Levels at Week 12
Description
The HDL-C will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Time Frame
12 weeks
Title
Systolic Blood Pressure at Week 12
Description
The systolic and blood pressure will be evaluated at baseline and at week 12 with a digital sphygmomanometer
Time Frame
12 weeks
Title
Diastolic Blood Pressure at Week 12.
Description
The diastolic and blood pressure will be evaluated at baseline and at week 12 with a digital sphygmomanometer
Time Frame
Baseline. Week 12
Title
Waist Circumference at Week 12
Description
The waist circumference will be evaluated at baseline and at week 12 with a flexible validated metric tape
Time Frame
12 weeks
Title
First Phase of Insulin Secretion at Week 12
Description
The first phase of insulin secretion will be calculated at baseline and week 12 with the stumvoll index from concentrations of glucose and insulin obtained of an oral glucose tolerance test. Human studies support the critical physiologic role of the first-phase of insulin secretion in the maintenance of postmeal glucose homeostasis. First phase of insulin secretion was estimated using the Stumvoll index (1283+ 1.829 x insulin 30' - 138.7 x glucose 30' + 3.772 x insulin 0'), the entered values reflect the first phase of insulin secretion
Time Frame
12 weeks
Title
Total Insulin Secretion at Week 12
Description
Total insulin secretion will be calculated at baseline and week 12 with the insulinogenic index from concentrations of glucose and insulin obtained of an oral glucose tolerance test. The insulinogenic index is a ratio that relates enhancement of circulating insulin to the magnitude of the corresponding glycemic stimulus. Total insulin secretion was calculated with the insulinogenic index (ΔABC insulin/ΔABC glucose), the entered values reflect the total insulin secretion
Time Frame
12 weeks
Title
Total Insulin Sensitivity at Week 12
Description
Insulin sensitivity will be calculated at baseline and week 12 with the stumvoll index from concentrations of glucose and insulin obtained of an oral glucose tolerance test. Matsuda Index value is used to indicate insulin resistance on diabetes. Insulin sensitivity was calculated with Matsuda index [10,000 / √glucose 0' x insulin 0') (mean glucose oral glucose tolerance test (OGTT) x mean insulin OGTT)]. The entered values reflect the insulin sensitivity
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Body Weight at Week 12
Description
The body weight will be measured at baseline and week 12 with a bioimpedance balance.
Time Frame
12 weeks
Title
Body Mass Index at Week 12
Description
The body mass index will be calculated at baseline and week 12 with the Quetelet index
Time Frame
12 weeks
Title
Total Cholesterol at Week 12
Description
Total cholesterol will be estimated bye standardized techniques at baseline and week 12
Time Frame
12 weeks
Title
Low Density Lipoproteins (LDL-C) at Week 12
Description
The LDL-C will be calculated at baseline and week 12 with the Friedewald formula
Time Frame
12 weeks
Title
Aspartate Aminotransferase at Week 12
Description
The aspartate aminotransferase will be determinated by standardized techniques at baseline and week 12
Time Frame
12 weeks
Title
Alanine Aminotransferase at Week 12
Description
The alanine aminotransferase will be determinated by standardized techniques at baseline and week 12
Time Frame
12 weeks
Title
Creatinine at Week 12
Description
Creatinine levels will be measured at baseline and week 12 with standardized techniques
Time Frame
12 weeks
Title
Uric Acid at Week 12
Description
Uric acid levels will be measured at baseline and week 12 with standardized techniques
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients both sexes Age between 30 and 60 years Metabolic syndrome according IDF modified criteria Waist circumference: Men ≥90 cm, women ≥80 cm And two of the following criteria: HDL-C: Men ≤40 mg/dL, women ≤50 mg/dL Fasting glucose ≥100 mg/dL Triglycerides ≥150 mg/dL Blood pressure ≥130/85 mmHg Informed consent signed Exclusion Criteria: Women with confirmed or suspected pregnancy Women under lactation and/or puerperium Known hypersensibility to Irvingia gabonensis Physical impossibility for taking pills Known uncontrolled renal, hepatic, heart or thyroid disease Previous treatment for the metabolic syndrome components Body mass index ≥ 39.9 kg/m2 Fasting glucose ≥126 mg/dL Triglycerides ≥ 500 mg/dL Total cholesterol ≥ 240 mg/dL LDL-C ≥190 mg/dL Blood pressure ≥140/90 mmHg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
MANUEL GONZALEZ, PhD
Organizational Affiliation
University of Guadalajara
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto de Terapéutica Experimental y Clínica
City
Guadalajara
State/Province
Jalisco
ZIP/Postal Code
44340
Country
Mexico

12. IPD Sharing Statement

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Effect of Irvingia Gabonensis Administration on Metabolic Syndrome, Insulin Secretion and Insulin Sensitivity

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