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Effect of Artemisia Dracunculus on Glucose Intolerance, Insulin Sensitivity and Insulin Secretion

Primary Purpose

Glucose Intolerance

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

About this trial

This is an interventional treatment trial for Glucose Intolerance focused on measuring Glucose Intolerance, Artemisia dracunculus, Insulin

Eligibility Criteria

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

Inclusion Criteria:

  • Patients both sexes
  • Age between 30 and 60 years
  • Glucose intolerance according ADA criteria (blood glucose leve ≥140 mg/dl and ≤199 mg/dL after an oral glucose tolerance test with 75 of oral glucose
  • Informed consent signed

Exclusion Criteria:

  • Women with confirmed or suspected pregnancy
  • Women under lactation and/or puerperium
  • Hypersensibility to Artemisia dracunculus
  • Physical impossibility for taking pills
  • Known uncontrolled renal, hepatic, heart or thyroid disease
  • Previous treatment for glucose
  • Diabetes diagnosis
  • BMI ≥39.9 kg/m2

Sites / Locations

  • Manuel González Ortiz

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Artemisia Dracunculus

Placebo

Arm Description

Artemisia Dracunculus extract, 2 capsules of 500 mg, two times per day before breakfast and dinner during 90 days

Calcined magnesia, 2 capsules of 500 mg, two times per day before breakfast and dinner during 90 days

Outcomes

Primary Outcome Measures

Postprandial Glucose Levels at Week 12
Postprandial glucose will be evaluated at baseline and week 12 after a oral glucose tolerance test with enzymatic-colorimetric techniques
Fasting Glucose Levels at Week 12
Fasting glucose will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Glycosylated Hemoglobin at Week 12
Glycosylated hemoglobin will be evaluated at baseline and week 12 by ELISA
First Phase of Insulin Secretion at Week 12
The first phase of insulin secretion will be calculated at baseline and week 12 with Stumvoll index. 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 insulinogenic index. 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
Insulin Sensitivity at Week 12
Insulin sensitivity will be calculated at baseline and week 12 with Matsuda index. 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

Weight at Week 12
The weight will be measured at baseline and week 12 with a bioimpedance balance
Body Mass Index at Week 12
Body Mass Index will be calculated at baseline and week 12 with the Quetelet index formula
Total Cholesterol at Week 12
Total cholesterol levels will be evaluated at baseline and week 12 by enzymatic-colorimetric techniques
Triglycerides Levels at Week 12
Triglycerides levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
High Density Lipoprotein (c-HDL) Levels at Week 12
c-HDL levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Alanine Aminotransferase (ALT) Levels at Week 12
ALT levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Aspartate Aminotransferase (AST) Levels at Week 12
AST levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Creatinine Levels at Week 12
Creatinine levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Uric Acid Levels at Week 12
Uric acid levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Systolic Blood Pressure at Week 12
Systolic blood pressure will be measured at baseline and week 12 with a digital sphygmomanometer
Diastolic Blood Pressure at Week 12.
Diastolic blood pressure will be measured at baseline and week 12 with a digital sphygmomanometer

Full Information

First Posted
December 30, 2014
Last Updated
September 11, 2020
Sponsor
University of Guadalajara
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1. Study Identification

Unique Protocol Identification Number
NCT02330341
Brief Title
Effect of Artemisia Dracunculus on Glucose Intolerance, Insulin Sensitivity and Insulin Secretion
Official Title
Effect of Artemisia Dracunculus on Glucose Intolerance, Insulin Sensitivity and Insulin Secretion
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
December 2014 (Actual)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
July 2015 (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 term prediabetes has been used to encompass the first alterations on glucose metabolism such as impaired fasting glucose and glucose intolerance, and its early detection and treatment could prevent the appearance of diabetes mellitus type 2, a high prevalence disease worldwide. Artemisia dracunculus, also known as estragon, has been used in Ayurvedic medicine for the treatment of diabetes. Different in vitro and in vivo studies have shown that Artemisia dracunculus increases insulin signaling and improves insulin sensitivity. The aim of this study is evaluate the effect of Artemisia dracunculus on glucose intolerance, insulin sensitivity and insulin secretion.
Detailed Description
A randomized, double-blind, placebo-controlled clinical trial will be carried out in 24 patients with diagnosis of glucose intolerance in accordance with the criteria of American Diabetes Association (ADA). Glucose, insulin levels, lipid profile, creatinine, uric acid, and transaminases will be evaluated. An oral glucose tolerance test with 75 g of dextrose will be held. 12 participants will receive Artemisia dracunculus, 1000 mg, twice per day (2000 mg) before breakfast and dinner during 3 months. And other 12 patients will receive placebo with the same prescription. Area Under de Curve of glucose and insulin will be calculated as well as total insulin secretion (insulinogenic index), first-phase of insulin secretion (Stumvoll index) and insulin sensitivity (Matsuda index). This protocol is approved by a local ethics committee and written informed consent will be obtained from all volunteers. Results will be presented as mean and standard deviation. Intra an inter group differences will be tested using the Wilcoxon signed-ran and Mann Whitney U- test respectively; p<0.05 will be considered significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glucose Intolerance
Keywords
Glucose Intolerance, Artemisia dracunculus, Insulin

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 prediabetes. One group received the investigational product (Artemisia Dracunculus) and the other received placebo as control.
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Artemisia Dracunculus
Arm Type
Experimental
Arm Description
Artemisia Dracunculus extract, 2 capsules of 500 mg, two times per day before breakfast and dinner during 90 days
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Calcined magnesia, 2 capsules of 500 mg, two times per day before breakfast and dinner during 90 days
Intervention Type
Dietary Supplement
Intervention Name(s)
Artemisia dracunculus
Other Intervention Name(s)
estragon, tarragon
Intervention Type
Other
Intervention Name(s)
Placebo
Other Intervention Name(s)
calcined magnesia
Primary Outcome Measure Information:
Title
Postprandial Glucose Levels at Week 12
Description
Postprandial glucose will be evaluated at baseline and week 12 after a oral glucose tolerance test with enzymatic-colorimetric techniques
Time Frame
Week 12
Title
Fasting Glucose Levels at Week 12
Description
Fasting glucose will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Time Frame
Week 12
Title
Glycosylated Hemoglobin at Week 12
Description
Glycosylated hemoglobin will be evaluated at baseline and week 12 by ELISA
Time Frame
Week 12
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 Stumvoll index. 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
Week 12
Title
Total Insulin Secretion at Week 12
Description
Total insulin secretion will be calculated at baseline and week 12 with insulinogenic index. 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
Week 12
Title
Insulin Sensitivity at Week 12
Description
Insulin sensitivity will be calculated at baseline and week 12 with Matsuda index. 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
Week 12
Secondary Outcome Measure Information:
Title
Weight at Week 12
Description
The weight will be measured at baseline and week 12 with a bioimpedance balance
Time Frame
Week 12
Title
Body Mass Index at Week 12
Description
Body Mass Index will be calculated at baseline and week 12 with the Quetelet index formula
Time Frame
Week 12
Title
Total Cholesterol at Week 12
Description
Total cholesterol levels will be evaluated at baseline and week 12 by enzymatic-colorimetric techniques
Time Frame
Week 12
Title
Triglycerides Levels at Week 12
Description
Triglycerides levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Time Frame
Week 12
Title
High Density Lipoprotein (c-HDL) Levels at Week 12
Description
c-HDL levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Time Frame
Week 12
Title
Alanine Aminotransferase (ALT) Levels at Week 12
Description
ALT levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Time Frame
Week 12
Title
Aspartate Aminotransferase (AST) Levels at Week 12
Description
AST levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Time Frame
Week 12
Title
Creatinine Levels at Week 12
Description
Creatinine levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Time Frame
Week 12
Title
Uric Acid Levels at Week 12
Description
Uric acid levels will be evaluated at baseline and week 12 with enzymatic-colorimetric techniques
Time Frame
Week 12
Title
Systolic Blood Pressure at Week 12
Description
Systolic blood pressure will be measured at baseline and week 12 with a digital sphygmomanometer
Time Frame
Week 12
Title
Diastolic Blood Pressure at Week 12.
Description
Diastolic blood pressure will be measured at baseline and week 12 with a digital sphygmomanometer
Time Frame
Week 12

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 Glucose intolerance according ADA criteria (blood glucose leve ≥140 mg/dl and ≤199 mg/dL after an oral glucose tolerance test with 75 of oral glucose Informed consent signed Exclusion Criteria: Women with confirmed or suspected pregnancy Women under lactation and/or puerperium Hypersensibility to Artemisia dracunculus Physical impossibility for taking pills Known uncontrolled renal, hepatic, heart or thyroid disease Previous treatment for glucose Diabetes diagnosis BMI ≥39.9 kg/m2
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
Manuel González Ortiz
City
Guadalajara
State/Province
Jalisco
ZIP/Postal Code
44140
Country
Mexico

12. IPD Sharing Statement

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Effect of Artemisia Dracunculus on Glucose Intolerance, Insulin Sensitivity and Insulin Secretion

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