Clinical Trials Directory

Trials / Completed

CompletedNCT03795792

Oral Curcumin Administration to Remit Metabolic Syndrome

Efficacy of Oral Curcumin Administration on Metabolic Syndrome Remission.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
105 (actual)
Sponsor
Coordinación de Investigación en Salud, Mexico · Other Government
Sex
All
Age
20 Years – 55 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTCurcuminWill be provided in capsules
DIETARY_SUPPLEMENTHydrolyzed collagenWill be provided in capsules.

Timeline

Start date
2018-05-06
Primary completion
2019-08-06
Completion
2019-12-06
First posted
2019-01-08
Last updated
2020-04-17

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT03795792. Inclusion in this directory is not an endorsement.