Effects of Resveratrol on Inflammation in Type 2 Diabetic Patients
Primary Purpose
Type 2 Diabetes Mellitus, Inflammation, Insulin Resistance
Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
resveratrol
Sponsored by
About this trial
This is an interventional treatment trial for Type 2 Diabetes Mellitus focused on measuring resveratrol, type 2 diabetes mellitus, inflammation, insulin resistance, body composition, bone mass
Eligibility Criteria
Inclusion Criteria:
- 35 years of age and older
- Type 2 diabetes with body mass index (BMI)<35 kg/m2
- Subjects on hypoglycemic agents other than insulin
- Willing to give written informed consent and able to understand, to participate in and to comply with the study requirements.
Exclusion Criteria:
- Subjects on any antioxidant medication
- Patient on non-steroidal anti-inflammatory drug, steroids or insulin
- On any agent with significant antioxidant properties
- History of drug or alcohol abuse
- Liver or kidney diseases
- Any life threatening diseases
- Allergy to peanuts, grapes, wine, mulberries
- Pregnant women
- Coronary event or procedure (myocardial infarction, unstable angina, coronary artery bypass surgery or coronary angioplasty) in the previous four Weeks
- Subjects on anticoagulants
Sites / Locations
- University of Turin
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Placebo Comparator
Experimental
Experimental
Arm Label
placebo
resveratrol 40
resveratrol 500
Arm Description
In this arm, 64 patients will receive a tablet of placebo once/day for 6 months
In this arm, 64 patients will receive a tablet of 40mg resveratrol once/day for 6 months
In this arm, 64 patients will receive a tablet of 500 mg resveratrol once/day for 6 months
Outcomes
Primary Outcome Measures
C reactive protein (CRP)
To investigate changes from baseline in blood concentrations of high-sensitivity CRP after six months of treatment with either resveratrol at different dosages or placebo
Secondary Outcome Measures
Metabolic and oxidative markers
To evaluate before-after changes in the concentrations of the following: Interleukin 6, Pentraxin-3, total antioxidant status, fasting glucose, insulin, glycated hemoglobin, total and HDL-cholesterol, triglycerides, adiponectin.
Full Information
NCT ID
NCT02244879
First Posted
September 15, 2014
Last Updated
March 6, 2016
Sponsor
University of Turin, Italy
Collaborators
Ministry of Health, Italy
1. Study Identification
Unique Protocol Identification Number
NCT02244879
Brief Title
Effects of Resveratrol on Inflammation in Type 2 Diabetic Patients
Official Title
Effects of Resveratrol on Inflammation in Type 2 Diabetic Patients. A Double-blind Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
October 2013 (undefined)
Primary Completion Date
February 2016 (Actual)
Study Completion Date
February 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Turin, Italy
Collaborators
Ministry of Health, Italy
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This research will investigate the effect of resveratrol on inflammatory mediators in type 2 diabetic patients in vivo.
The investigators will also investigate the hypothesis that resveratrol has an antioxidant activity, improves insulin sensitivity and lipid pattern, down-regulates bone-turnover.
Detailed Description
Despite a large body of evidence demonstrating promising effects of resveratrol in rodents, human studies are still lacking and both preventive and therapeutic value of resveratrol in humans remains to be elucidated. The published evidence is not sufficiently strong to recommend for the administration of resveratrol to humans, beyond dietary sources. On the other hand, animal data are promising in prevention of various cancer types, coronary heart diseases and diabetes which strongly indicate the need for human clinical trials.
Furthermore, data are lacking either about safety during long-term administration, or on the efficacy of resveratrol administration in patients with chronic illnesses, such as diabetes mellitus.
The main objective of this study is to investigate the effect of resveratrol on inflammatory mediators in type 2 diabetic patients in vivo.
This research will investigate the hypothesis that resveratrol, when given orally to type 2 diabetic subjects for 24 weeks induces a decrease in values of high-sensitivity CRP (C-reactive protein) (primary outcome measure), IL-6 (Interleukin-6), PTX3 (pentraxin 3).
The investigators will also investigate the hypothesis that resveratrol has an antioxidant activity, improves insulin sensitivity and lipid pattern, down-regulates bone-turnover. Secondary outcomes are therefore variations in the following variables: TAS (total antioxidant status), glycemia, glycated hemoglobin (HbA1c), Homeostasis model assessment of insulin resistance (HOMA-IR), total and HDL-cholesterol, triglycerides, adiponectin, body composition (evaluated by Dual-emission X-ray absorptiometry DXA-), bone mineral density (DXA).
Finally, the investigators are interested in evaluating efficacy, safety and tolerability of two different dosages of resveratrol: 500 mg/day and 40 mg/day.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus, Inflammation, Insulin Resistance, Other Disorders of Bone Density and Structure
Keywords
resveratrol, type 2 diabetes mellitus, inflammation, insulin resistance, body composition, bone mass
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
192 (Actual)
8. Arms, Groups, and Interventions
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
In this arm, 64 patients will receive a tablet of placebo once/day for 6 months
Arm Title
resveratrol 40
Arm Type
Experimental
Arm Description
In this arm, 64 patients will receive a tablet of 40mg resveratrol once/day for 6 months
Arm Title
resveratrol 500
Arm Type
Experimental
Arm Description
In this arm, 64 patients will receive a tablet of 500 mg resveratrol once/day for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
resveratrol
Intervention Description
arm resveratrol 500: 6 months of resveratrol 500 mg/day arm resveratrol 40: 6 months of resveratrol 40 mg/day
Primary Outcome Measure Information:
Title
C reactive protein (CRP)
Description
To investigate changes from baseline in blood concentrations of high-sensitivity CRP after six months of treatment with either resveratrol at different dosages or placebo
Time Frame
up to 25 months
Secondary Outcome Measure Information:
Title
Metabolic and oxidative markers
Description
To evaluate before-after changes in the concentrations of the following: Interleukin 6, Pentraxin-3, total antioxidant status, fasting glucose, insulin, glycated hemoglobin, total and HDL-cholesterol, triglycerides, adiponectin.
Time Frame
up to 25 months
Other Pre-specified Outcome Measures:
Title
body composition and bone mineral density
Description
To evaluate before-after change in bone mineral density and body composition by Dual-emission X-ray absorptiometry
Time Frame
up to 25 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
35 years of age and older
Type 2 diabetes with body mass index (BMI)<35 kg/m2
Subjects on hypoglycemic agents other than insulin
Willing to give written informed consent and able to understand, to participate in and to comply with the study requirements.
Exclusion Criteria:
Subjects on any antioxidant medication
Patient on non-steroidal anti-inflammatory drug, steroids or insulin
On any agent with significant antioxidant properties
History of drug or alcohol abuse
Liver or kidney diseases
Any life threatening diseases
Allergy to peanuts, grapes, wine, mulberries
Pregnant women
Coronary event or procedure (myocardial infarction, unstable angina, coronary artery bypass surgery or coronary angioplasty) in the previous four Weeks
Subjects on anticoagulants
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simona Bo, MD
Organizational Affiliation
University of Turin, Italy
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Turin
City
Turin
State/Province
IT
ZIP/Postal Code
10126
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
29330620
Citation
Bo S, Togliatto G, Gambino R, Ponzo V, Lombardo G, Rosato R, Cassader M, Brizzi MF. Impact of sirtuin-1 expression on H3K56 acetylation and oxidative stress: a double-blind randomized controlled trial with resveratrol supplementation. Acta Diabetol. 2018 Apr;55(4):331-340. doi: 10.1007/s00592-017-1097-4. Epub 2018 Jan 12.
Results Reference
derived
PubMed Identifier
28238190
Citation
Bo S, Ponzo V, Evangelista A, Ciccone G, Goitre I, Saba F, Procopio M, Cassader M, Gambino R. Effects of 6 months of resveratrol versus placebo on pentraxin 3 in patients with type 2 diabetes mellitus: a double-blind randomized controlled trial. Acta Diabetol. 2017 May;54(5):499-507. doi: 10.1007/s00592-017-0977-y. Epub 2017 Feb 25.
Results Reference
derived
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Effects of Resveratrol on Inflammation in Type 2 Diabetic Patients
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