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Supplementation of Eriocitrin in Intestinal Microbiota

Primary Purpose

Pre Diabetes

Status
Terminated
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Eriocitrin
Sponsored by
São Paulo State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pre Diabetes focused on measuring Eriocitrin, Citrus bioflavonoids, Flavanone, Pre-diabetes, Blood glucose, Microbiome

Eligibility Criteria

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

Inclusion Criteria:

  • 30-60 years
  • Increased fasting blood glucose from 6.1 to 7.0 mmol / L or,
  • Decreased glucose tolerance of 7 , 8 to 11.1 mmol / L or,
  • Glycated hemoglobin with values between 5.7 and 6.4%

Exclusion Criteria:

  • Use hypoglycemic, hypolipidemic drugs,
  • Use dietary supplements (vitamins, minerals, bioflavonoids, prebiotics, probiotics or other bioactive compounds),
  • Exercise intensely (more than 10 hours per week)
  • History of cardiovascular diseases , diabetes mellitus, liver and kidney disease.

Sites / Locations

  • Sao Paulo State University "Julio de Mesquita Filho"

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

No Intervention

Arm Label

Eriomin 200 mg

Eriomin 400 mg

Eriomin 800 mg

Placebo

Arm Description

The volunteers will receive one capsule containing 200 mg eriocitrin

The volunteers will receive one capsule containing 400 mg eriocitrin

The volunteers will receive one capsule containing 800 mg eriocitrin

The volunteers will receive a capsule containing corn starch (placebo)

Outcomes

Primary Outcome Measures

Rate of change in microbiome
Changes in microbiome before and after administration of the intervention / placebo

Secondary Outcome Measures

Rate of change in plasma glucose concentration
Changes in serum 2 hours after oral glucose tolerance test, HbA1c, insulin, HOMA-IR before and after administration of the intervention / placebo

Full Information

First Posted
April 17, 2019
Last Updated
March 24, 2020
Sponsor
São Paulo State University
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1. Study Identification

Unique Protocol Identification Number
NCT03925909
Brief Title
Supplementation of Eriocitrin in Intestinal Microbiota
Official Title
Effect of Chronic Eriocitrin Supplementation on the Intestinal Microbiota of Pre-diabetic and Insulin Resistant Individuals
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Terminated
Why Stopped
Because there was no funding
Study Start Date
May 1, 2019 (Actual)
Primary Completion Date
August 1, 2019 (Actual)
Study Completion Date
March 23, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
São Paulo State University

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
Pre-diabetes is characterized by high plasma concentration of glucose and glycated hemoglobin and is the main risk factor for the development of type 2 diabetes. Several studies show that the intestinal microbiota is intimately linked to cardio-metabolic factors (type 2 diabetes, insulin resistance) when in situations of dysbiosis. Food is a key element for a healthy microbiota, focusing on the consumption of polyphenols that modulate the intestinal environment through its alteration and production of short chain fatty acids, and can thus be a way of reversing situations such as pre- diabetes and insulin resistance. The objective of the study will be to investigate whether chronic supplementation of eriocitrin alters the intestinal microbiota of pre-diabetic and insulin resistant individuals, reversing these situations. This will be done by supplementation of eriocitrin-containing capsules with different dosages in pre-diabetic and insulin resistant individuals. There will be 12 weeks of intervention, with faecal collections, anthropometric and dietary evaluation, and then will be made microbiological analysis to identify the intestinal microbiota and biochemical analysis before and after the intervention. For statistical analysis, normality and homogeneity test (Kolmogorov-Smirnov and Levine test respectively), T-test to compare baseline time between groups and repeated-measures ANOVA (two-way) were used to compare changes within and between groups.
Detailed Description
Individuals of both sexes between 30 and 60 years of age who present fasting glycemia between 100 mg / dL (5,6 mmol / L) and 125 mg / dL (6,9 mmol / L) 50, or concentration of glycated hemoglobin between 5.7% (39 mmol / mole) and 6.4% (47 mmol / mole) 50, or glycemic concentrations in the oral glucose tolerance test between 140mg / dL (7.8 mmol / L) to 199mg / dL (11.0 mmol / L) 50. The study will also include insulin-resistant individuals: insulin above 25 uU / mL, or who present HOMA-IR score above 2.7. Individuals using supplements (vitamins, bioflavonoids), pregnant women and those who practice intense physical exercise (> 10h / week) will be excluded from the study. The primary endpoint will be alteration of the microbiota with possible improvement of the glycemic profile, leading to the reversal of pre-diabetes and insulin resistance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pre Diabetes
Keywords
Eriocitrin, Citrus bioflavonoids, Flavanone, Pre-diabetes, Blood glucose, Microbiome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Eriomin 200 mg
Arm Type
Experimental
Arm Description
The volunteers will receive one capsule containing 200 mg eriocitrin
Arm Title
Eriomin 400 mg
Arm Type
Experimental
Arm Description
The volunteers will receive one capsule containing 400 mg eriocitrin
Arm Title
Eriomin 800 mg
Arm Type
Experimental
Arm Description
The volunteers will receive one capsule containing 800 mg eriocitrin
Arm Title
Placebo
Arm Type
No Intervention
Arm Description
The volunteers will receive a capsule containing corn starch (placebo)
Intervention Type
Dietary Supplement
Intervention Name(s)
Eriocitrin
Intervention Description
The responsible nutritionists will do 1) Anthropometric Assessment, in which weight data will be collected (kg); height (m); waist circumference (cm), waist circumference (cm) and hip circumference (cm), muscle mass (kg /%) and percentage of fat by means of bioimpedance equipment; 2) Dietary assessment, which will be performed through a 24-hour Food Recall, a 3-day Food Record and a Food Consumption Frequency Questionnaire; 3) Evaluation of the microbiota, for which stool will be collected from the last 24 hours on the day before the beginning of the experiment and at the end of the study (week 12); 3) Biochemical evaluation, which includes the collection of 30 mL of blood to be performed by trained and qualified technicians.
Primary Outcome Measure Information:
Title
Rate of change in microbiome
Description
Changes in microbiome before and after administration of the intervention / placebo
Time Frame
0-12 week
Secondary Outcome Measure Information:
Title
Rate of change in plasma glucose concentration
Description
Changes in serum 2 hours after oral glucose tolerance test, HbA1c, insulin, HOMA-IR before and after administration of the intervention / placebo
Time Frame
0-12 week

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: 30-60 years Increased fasting blood glucose from 6.1 to 7.0 mmol / L or, Decreased glucose tolerance of 7 , 8 to 11.1 mmol / L or, Glycated hemoglobin with values between 5.7 and 6.4% Exclusion Criteria: Use hypoglycemic, hypolipidemic drugs, Use dietary supplements (vitamins, minerals, bioflavonoids, prebiotics, probiotics or other bioactive compounds), Exercise intensely (more than 10 hours per week) History of cardiovascular diseases , diabetes mellitus, liver and kidney disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thais B Cesar, Phd
Organizational Affiliation
ao Paulo State University "Julio de Mesquita Filho"
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sao Paulo State University "Julio de Mesquita Filho"
City
Araraquara
State/Province
SP
ZIP/Postal Code
14800-903
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Supplementation of Eriocitrin in Intestinal Microbiota

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