Oral Curcumin Administration to Remit Metabolic Syndrome
Primary Purpose
Metabolic Syndrome
Status
Completed
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Curcumin
Hydrolyzed collagen
Sponsored by
About this trial
This is an interventional treatment trial for Metabolic Syndrome
Eligibility Criteria
Inclusion Criteria:
- Women and men.
- 20 to 55 years old.
- Diagnosis of metabolic syndrome according to the ATP III criteria.
- Informed consent of the participant.
Exclusion Criteria:
- Diabetes or hypoglycaemic therapy.
- High blood pressure o anti-hypertensive treatments.
- Hypertriglyceridemia (>400 g/dL) or lipid lowering treatment.
- Neoplasia disease.
- Thyroid disease
- Syndrome of polycystic ovary.
- Pregnancy or lactation.
- Smoking.
- Anti-inflammatory medicines in the last two months.
- Food supplements in the last two months.
Sites / Locations
- Biomedical Research Unit. IMSS. Durango
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Curcumin
Hydrollased collagen
Arm Description
Curcumin 1.2 g / black pepper 10 mg a day for 3 months, plus recommendations to decrease calories intake and do exercise.
Hydrolyzed collagen 1.2 g / black pepper 10 mg a day for 3 months, plus recommendations to decrease calories intake and do exercise.
Outcomes
Primary Outcome Measures
Remission of metabolic syndrome.
Presence of two or less metabolic syndrome criteria, according to the ATP III criteria.
Secondary Outcome Measures
Full Information
NCT ID
NCT03795792
First Posted
January 4, 2019
Last Updated
April 16, 2020
Sponsor
Coordinación de Investigación en Salud, Mexico
1. Study Identification
Unique Protocol Identification Number
NCT03795792
Brief Title
Oral Curcumin Administration to Remit Metabolic Syndrome
Official Title
Efficacy of Oral Curcumin Administration on Metabolic Syndrome Remission.
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
May 6, 2018 (Actual)
Primary Completion Date
August 6, 2019 (Actual)
Study Completion Date
December 6, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Coordinación de Investigación en Salud, Mexico
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 consists of a set of risk factors that increases the probability to develop heart diseases and type 2 diabetes, two of the principal chronic diseases that affect Mexican population. The curcumin is a compound that is extracted from the root of a plant called Cúrcuma longa. There exists information that curcumin helps to diminish weight and the levels of blood glucose and blood fats. The hypothesis of this study is: that curcumin administration combined with diet and exercise remits the metabolic syndrome.
Detailed Description
Objective: The aim of this study is to determinate the efficacy of oral administration of curcumin in the remission of metabolic syndrome.
Design: clinical trial, randomized, double blind, placebo controlled.
Study population: Men and women from 20 to 55 years old with metabolic syndrome according to the ATP III criteria, will be included.
Study groups: intervention and control group.
Sample size: It was calculated using a statistical power of 80%, an alpha value of 0.05. A 50% of the difference in the mean of remission of metabolic syndrome between control group and intervention groups was considered. The estimated sample size was 220 subjects for each group.
Process: All eligible participants according to inclusion and exclusion criteria, will be randomized to one of the study groups.
The intervention group will receive a total dose of curcumin 1.2 g / black pepper 10 mg a day; and control group will receive a total dose of hydrolyzed collagen 1.2 g / black pepper 10 mg a day; plus dietary and exercise recommendations for both groups during three months.
The blood concentrations of glucose, triglycerides, and HDL cholesterol will be measured, as well as the abdominal perimeter and blood pressure, at baseline conditions, at one month and three months after treatment.
Statistical analysis: Numerical values will be expressed as mean ± standard deviation; categorical variables will be expressed as proportions. Differences between the groups were estimated by unpaired Student t test for numerical variables (Mann-Whitney U test for skewed data) or Chi-square and Fisher´s exact test for categorical variables. Intragroup differences were estimated by paired Student t-test.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Study groups:
Intervention group: curcumin 1.2 g / black pepper 10 mg a day for 3 months, plus recommendations to decrease calories intake and do exercise.
Control group: hydrolyzed collagen 1.2 g / black pepper 10 mg a day for 3 months, plus recommendations to decrease calories intake and do exercise.
Masking
ParticipantCare Provider
Masking Description
Neither the patient nor the treating doctor will know the study group the participant was randomized.
Allocation
Randomized
Enrollment
105 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Curcumin
Arm Type
Experimental
Arm Description
Curcumin 1.2 g / black pepper 10 mg a day for 3 months, plus recommendations to decrease calories intake and do exercise.
Arm Title
Hydrollased collagen
Arm Type
Placebo Comparator
Arm Description
Hydrolyzed collagen 1.2 g / black pepper 10 mg a day for 3 months, plus recommendations to decrease calories intake and do exercise.
Intervention Type
Dietary Supplement
Intervention Name(s)
Curcumin
Other Intervention Name(s)
Turmeric
Intervention Description
Will be provided in capsules
Intervention Type
Dietary Supplement
Intervention Name(s)
Hydrolyzed collagen
Intervention Description
Will be provided in capsules.
Primary Outcome Measure Information:
Title
Remission of metabolic syndrome.
Description
Presence of two or less metabolic syndrome criteria, according to the ATP III criteria.
Time Frame
Three months.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Women and men.
20 to 55 years old.
Diagnosis of metabolic syndrome according to the ATP III criteria.
Informed consent of the participant.
Exclusion Criteria:
Diabetes or hypoglycaemic therapy.
High blood pressure o anti-hypertensive treatments.
Hypertriglyceridemia (>400 g/dL) or lipid lowering treatment.
Neoplasia disease.
Thyroid disease
Syndrome of polycystic ovary.
Pregnancy or lactation.
Smoking.
Anti-inflammatory medicines in the last two months.
Food supplements in the last two months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fernando Guerrero, PhD
Organizational Affiliation
Instituto Mexicano del Seguro Social
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Luis Simental, PhD
Organizational Affiliation
Instituto Mexicano del Seguro Social
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Gerardo Martínez, PhD
Organizational Affiliation
Instituto Mexicano del Seguro Social
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Claudia Gamboa, PhD
Organizational Affiliation
Instituto Mexicano del Seguro Social
Official's Role
Study Chair
Facility Information:
Facility Name
Biomedical Research Unit. IMSS. Durango
City
Durango
State/Province
Dgo
ZIP/Postal Code
34067
Country
Mexico
12. IPD Sharing Statement
Plan to Share IPD
No
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Oral Curcumin Administration to Remit Metabolic Syndrome
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