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Effect of Administration of Resveratrol on Glycemic Variability in Individuals With Type 2 Diabetes Mellitus

Effect of Administration of Resveratrol on Glycemic Variability in Individuals With Type 2 Diabetes Mellitus Inadequately Controlled With Metformin

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02549924
Enrollment
22
Registered
2015-09-15
Start date
2016-09-30
Completion date
2018-02-01
Last updated
2018-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes Mellitus

Keywords

Resveratrol, Glycemic Variability, MAGE

Brief summary

Type 2 diabetes mellitus \[ T2DM \] has quickly become the epidemic of the XXI century and challenging global health . Estimates of the World Health Organization \[ WHO \] indicate that globally , from 1995 to date has nearly tripled the number of people living with diabetes mellitus \[DM \]. Resveratrol has been extensively studied as a regulator of glucose through its antioxidant effects and protecting pancreatic β cells by activation of sirtuin -1 \[ SIRT1 \] dependent deacetylase nicotinamide adenine diphosphate \[ NAD \]. Therefore, it is important to know the effect of resveratrol on the glycemic variability \[GV \] in patients with T2DM who are not in control with metformin monotherapy based.

Detailed description

The objective is to evaluate the effect of administration of resveratrol on GV in individuals with T2DM inadequately controlled on metformin, for which we will conduct a double-blind trial, randomized, placebo control group, each group 11 male and female patients 30-60 years of age with T2DM inadequately controlled with metformin \[2000 mg / day and glycosylated hemoglobin A1c (A1C) ≥% 7\], with body mass index \[BMI\] form 25.0 to 34.9 kg / m2. Randomization will determine who will receive the intervention during the 8-week trial \[resveratrol capsules, 500 mg 3 times daily with the first bite of each meal or approved placebo capsules\], both groups also continue with metformin. The clinical findings and laboratory tests include a metabolic profile and biosafety, which will be made at baseline and at 8 weeks. Body weight, body fat, BMI and blood pressure will be determined during the initial and final visit, likewise, plasma glucose concentrations every hour recorded over 72 hours by continuous monitoring system outpatient glucose \[MACG\] via iPro ™ 2 \[Medtronic MiniMed, Northridge\] system, through which the mean amplitude of glucose excursions \[MAGE\] is calculated and AUC glucose, which will serve to assess the GV. Adverse events and adherence to treatment will be documented. Statistical analysis: Mann-Whitney U test, Wilcoxon and Fisher exact test. It is considered with significance at p \<0.05.

Interventions

DRUGResveratrol

Resveratrol capsules, 500 mg 3 times daily with the first bite of each meal

DRUGPlacebo

Placebo capsules, 500 mg 3 times daily with the first bite of each meal

Sponsors

University of Guadalajara
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* BMI from 25.0-34.9 kg/m2 * Diagnosis of T2DM * Fasting plasma glucose \>130 and \<250 mg/dl at the time of scrutiny * A1C between 7 and 10% * Metformin monotherapy * Written informed consent

Exclusion criteria

* Women pregnant or breastfeeding * Untreated thyroid disease and/or uncontrolled hypertension \[≥150 systolic and diastolic ≥90\] * Consumption of oral agents or other medications or supplements, unlike metformin, with proven properties that modify the behavior of glucose * Total cholesterol \>400 mg/dL * Triglycerides ≥400 mg/dL * Liver enzymes \[ALT and AST\] more than twice the normal range * Glomerular filtration rate \<60 mL/min \[Cockcroft-Gault\]

Design outcomes

Primary

MeasureTime frameDescription
Area under the curve56 daysBefore and after intervention with ambulatory continuous glucose monitoring during 72 h, oxidase glucose iPro ™ 2
Mean amplitude of glucose excursions (MAGE)56 daysBefore and after intervention with ambulatory continuous glucose monitoring during 72 h, oxidase glucose iPro ™ 2

Secondary

MeasureTime frameDescription
A1C56 daysBefore and after intervention by high-performance liquid chromatography
Total cholesterol56 daysBefore and after intervention by spectrophotometry
Triglycerides56 daysBefore and after intervention by spectrophotometry
High-density lipoprotein cholesterol56 daysBefore and after intervention by spectrophotometry
Low-density lipoprotein cholesterol56 daysFriedewald formula
Fasting plasma glucose56 daysBefore and after intervention by spectrophotometry
Alanine aminotransferase56 daysBefore and after intervention by spectrophotometry
Aspartate aminotransferase56 daysBefore and after intervention by spectrophotometry
Creatinine56 daysBefore and after intervention by spectrophotometry
Blood pressure56 daysBefore and after intervention using a digital manometer
Body and visceral fat %56 daysBefore and after intervention using a impedance bascule, Tanita MR
Very-low density lipoprotein56 daysFriedewald formula
Postprandial glucose56 daysBefore and after intervention with ambulatory continuous glucose monitoring during 72 h, oxidase glucose iPro ™ 2

Countries

Mexico

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026