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Effect of Oral Supplementation With Curcumin on Insulin Sensitivity in Subjects With Prediabetes

Primary Purpose

PreDiabetes

Status
Unknown status
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
Curcumin
Starch
Sponsored by
Hospital General de México Dr. Eduardo Liceaga
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for PreDiabetes focused on measuring Curcumin, Insulin sensitivity, HOMA

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Men and women with age between 18 and 60 years old.
  • With prediabetes diagnosis, according to the American Diabetes Association :

    1. Fasting serum glucose: 100-125 mg/dL
    2. Glycosylated hemoglobin (HbA1c): 5.7-6.4%
    3. Post-prandial glucose: 140-199 mg/dL after an oral dose of 75 g of glucose.

Exclusion Criteria:

  • Subjects with any type of diabetes.
  • Subjects with body mass index > 35 kg/m2
  • Pregnant Women.
  • Volunteers who ingest drugs that alter blood glucose levels, antiplatelet agents, angiotensin-converting enzyme inhibitors, angiotensin II receptor antagonists, fibrates, statins.
  • Subjects with serum creatinine > 2 mg/dL or in renal replacement therapy.
  • Subjects that normally consume food supplements.
  • Subjects with acute infections or with chronical diseases (cancer, rheumatoid arthritis, etc.).

Sites / Locations

  • Hospital General de México Dr. Eduardo LiceagaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Curcumin and bioperine

Placebo

Arm Description

This group will receive curcumin 500 mg and bioperine 5 mg oral dosing every 12 hours for 3 months

This group will receive placebo (starch) 500 mg oral dosing every 12 hours for 3 months

Outcomes

Primary Outcome Measures

HOMA- IR
(Insulin µU/ml)(Glucose mg/dl)/405.
HOMA- Beta
(20)(FPI)/(FPG - 3.5)
Matsuda index
10,000/√[(basal glucose)(basal insulin)*(glucose)(insulin)]

Secondary Outcome Measures

weight
weight in kilograms
height
height in centimetres
waist circumference
waist circumference in centimetres
hip circumference.
hip circumference in centimetres
insulin
insulin in µU/ml
triglycerides
triglycerides in mg/dl
cholesterol
cholesterol in mg/dl
HDL cholesterol
HDL cholesterol in mg/dl
LDL cholesterol
LDL cholesterol in mg/dl
uric acid
uric acid in mg/dl
creatinine
creatinine in mg/dl
urea
urea in mg/dl
alanine amino transferase
alanine amino transferase in U/L
alkaline phosphatase
alkaline phosphatase in U/L
lactic dehydrogenase
lactic dehydrogenase in U/L
glycosylated hemoglobin
glycosylated hemoglobin in percentage
total bilirubin
total bilirubin in mg/dl

Full Information

First Posted
April 7, 2019
Last Updated
April 13, 2019
Sponsor
Hospital General de México Dr. Eduardo Liceaga
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1. Study Identification

Unique Protocol Identification Number
NCT03917784
Brief Title
Effect of Oral Supplementation With Curcumin on Insulin Sensitivity in Subjects With Prediabetes
Official Title
Effect of Oral Supplementation With Curcumin on Insulin Sensitivity in Subjects With Prediabetes
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Unknown status
Study Start Date
February 25, 2019 (Actual)
Primary Completion Date
November 30, 2019 (Anticipated)
Study Completion Date
February 28, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital General de México Dr. Eduardo Liceaga

4. Oversight

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

5. Study Description

Brief Summary
This study evaluates the effects of oral supplementation with curcumin on the insulin sensitivity in subjects with prediabetes. The half of participants will receive curcumin and bioperine in combination, while the other half receive placebo.
Detailed Description
The therapeutic strategies for prediabetes to this day are based on the change of habits, mainly food and exercise plans. It has been advice, in specific circumstances, to grant a pharmacological regimen. Curcumin or Curcuma Longa ((1E,6E)21,7-bis(4-hydroxy-3-methoxyphenyl)-1,6- heptadiene-3,5-dione), is the main ingredient of the Hindu condiment, Turmeric, which is obtained from the Rhizome plant. In new studies, it has been documented that the oral consumption of curcumin (Curcuma longa) in pre-diabetic and diabetic patients has a positive effect as an antidiabetic agent thanks to its anti-inflammatory, antioxidant, antithrombotic, cardio and neuroprotective effects. In animal models, it has been shown that oral curcumin consumption is capable of increasing insulin sensitivity in liver, muscle and adipose tissue, increases glucose uptake in muscle and insulin secretion, which is reflected in the reduction of hyperglycemia, glycosylated hemoglobin, decrease of the homeostatic model assessment of insulin resistance (HOMA-IR) and decrease of serum lipids. Curcumin has been included in the oriental diet since ancient times and is used in traditional medicine, which is why it is considered safe, since its consumption is approved by the FDA (Federal Drugs Administration). A 12g per day dose has shown no side effects in humans. Therefore, it is proposed that the consumption of curcumin in pre-diabetic patients can improve glucose tolerance and decrease insulin resistance parameters.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PreDiabetes
Keywords
Curcumin, Insulin sensitivity, HOMA

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized, double-blind, placebo-controlled clinical trial.
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
142 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Curcumin and bioperine
Arm Type
Experimental
Arm Description
This group will receive curcumin 500 mg and bioperine 5 mg oral dosing every 12 hours for 3 months
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
This group will receive placebo (starch) 500 mg oral dosing every 12 hours for 3 months
Intervention Type
Drug
Intervention Name(s)
Curcumin
Intervention Description
Oral supplementation with curcumin 500 mg oral dosing for 3 months
Intervention Type
Drug
Intervention Name(s)
Starch
Intervention Description
Oral supplementation with starch 500 mg oral dosing for 3 months
Primary Outcome Measure Information:
Title
HOMA- IR
Description
(Insulin µU/ml)(Glucose mg/dl)/405.
Time Frame
3 months
Title
HOMA- Beta
Description
(20)(FPI)/(FPG - 3.5)
Time Frame
3 months
Title
Matsuda index
Description
10,000/√[(basal glucose)(basal insulin)*(glucose)(insulin)]
Time Frame
3 months
Secondary Outcome Measure Information:
Title
weight
Description
weight in kilograms
Time Frame
6 weeks and 12 weeks
Title
height
Description
height in centimetres
Time Frame
6 weeks and 12 weeks
Title
waist circumference
Description
waist circumference in centimetres
Time Frame
6 weeks and 12 weeks
Title
hip circumference.
Description
hip circumference in centimetres
Time Frame
6 weeks and 12 weeks
Title
insulin
Description
insulin in µU/ml
Time Frame
6 weeks and 12 weeks
Title
triglycerides
Description
triglycerides in mg/dl
Time Frame
6 weeks and 12 weeks
Title
cholesterol
Description
cholesterol in mg/dl
Time Frame
6 weeks and 12 weeks
Title
HDL cholesterol
Description
HDL cholesterol in mg/dl
Time Frame
6 weeks and 12 weeks
Title
LDL cholesterol
Description
LDL cholesterol in mg/dl
Time Frame
6 weeks and 12 weeks
Title
uric acid
Description
uric acid in mg/dl
Time Frame
6 weeks and 12 weeks
Title
creatinine
Description
creatinine in mg/dl
Time Frame
6 weeks and 12 weeks
Title
urea
Description
urea in mg/dl
Time Frame
6 weeks and 12 weeks
Title
alanine amino transferase
Description
alanine amino transferase in U/L
Time Frame
6 weeks and 12 weeks
Title
alkaline phosphatase
Description
alkaline phosphatase in U/L
Time Frame
6 weeks and 12 weeks
Title
lactic dehydrogenase
Description
lactic dehydrogenase in U/L
Time Frame
6 weeks and 12 weeks
Title
glycosylated hemoglobin
Description
glycosylated hemoglobin in percentage
Time Frame
6 weeks and 12 weeks
Title
total bilirubin
Description
total bilirubin in mg/dl
Time Frame
6 weeks and 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Men and women with age between 18 and 60 years old. With prediabetes diagnosis, according to the American Diabetes Association : Fasting serum glucose: 100-125 mg/dL Glycosylated hemoglobin (HbA1c): 5.7-6.4% Post-prandial glucose: 140-199 mg/dL after an oral dose of 75 g of glucose. Exclusion Criteria: Subjects with any type of diabetes. Subjects with body mass index > 35 kg/m2 Pregnant Women. Volunteers who ingest drugs that alter blood glucose levels, antiplatelet agents, angiotensin-converting enzyme inhibitors, angiotensin II receptor antagonists, fibrates, statins. Subjects with serum creatinine > 2 mg/dL or in renal replacement therapy. Subjects that normally consume food supplements. Subjects with acute infections or with chronical diseases (cancer, rheumatoid arthritis, etc.).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
César L González
Phone
01 993 117 1322
Email
celsbca_21033@hotmail.com
Facility Information:
Facility Name
Hospital General de México Dr. Eduardo Liceaga
City
Mexico City
State/Province
Cuauhtémoc
ZIP/Postal Code
06720
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ernesto Roldan
Phone
2789-2000
Ext
1164
Email
ernest.roldan@usa.net

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Identified individual participant data for all primary and secondary outcomes measures will be made avaliable
IPD Sharing Time Frame
Data will be avaliable whithin 6 months of study completion
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Effect of Oral Supplementation With Curcumin on Insulin Sensitivity in Subjects With Prediabetes

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