Status:

COMPLETED

Resveratrol Stimulates Insulin Sensitivity in Subjects With Obesity and Insulin Resistance

Lead Sponsor:

Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

Conditions:

Obesity

Eligibility:

All Genders

20-60 years

Phase:

NA

Brief Summary

There is evidence that resveratrol can improve insulin resistance in rodents and humans with obesity and it can also improve muscle mitochondrial content mediated through activation of AMPK. However, ...

Detailed Description

The investigators included 38 participants who met the following inclusion criteria: adults between 20 and 60 years of age with a diagnosis of HOMA-IR index greater than 2.5, and BMI ≥30 and ≤ 40 kg /...

Eligibility Criteria

Inclusion

  • Male and female.
  • Between 20 and 60 years
  • BMI ≥ 30 and ≤ 40 kg/m2
  • Presence of insulin resistance (HOMA-IR index ≥ 2.5)
  • Willing and able to sign written informed consent prior to trial entry

Exclusion

  • Patients with any type of diabetes.
  • Patients with kidney disease diagnosed by a medical or with creatinine\> 1.3 mg / dL for men and \> 1.1 mg / dL for women and / or BUN\> 20 mg / dL.
  • Patients with acquired diseases that produce obesity and diabetes secondarily.
  • Patients who have suffered a cardiovascular event.
  • Patients with gastrointestinal diseases.
  • Weight loss \> 3 kg in the last 3 months.
  • Catabolic diseases such as cancer and acquired immunodeficiency syndrome.
  • Pregnancy status.
  • Antibiotic consumption 3 months prior to the study.
  • Be an undergraduate or graduate student within the Institute.
  • Positive smoking.
  • Drug treatment:
  • Antihypertensive drugs or treatment
  • Treatment with hypoglycemic agents or insulin and antidiabetic drugs.
  • Treatment with statins, fibrates or other drugs to control dyslipidemia.
  • Use of antibiotics in the three months prior to the study.
  • Use of steroid drugs, chemotherapy, immunosuppressants, or radiation therapy.
  • Anorexigenic or that accelerate weight loss such as sibutramine or orlistat.
  • Probiotic, prebiotic or symbiotic supplements.

Key Trial Info

Start Date :

September 15 2013

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2018

Estimated Enrollment :

38 Patients enrolled

Trial Details

Trial ID

NCT06961279

Start Date

September 15 2013

End Date

December 1 2018

Last Update

May 13 2025

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubiran

Mexico City, Mexico