Mechanisms of Metabolic Regulation of Resveratrol on Humans With Metabolic Syndrome (RSV)
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ClinicalTrials.gov Identifier: NCT00654667 |
Recruitment Status :
Withdrawn
(no participant enrollment)
First Posted : April 9, 2008
Last Update Posted : March 4, 2015
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Insulin Resistance | Drug: Placebo Drug: Resveratrol | Phase 2 |
Hypotheses for this study:
4 weeks of supplementation with RSV 5.0 grams daily compared to placebo control in individuals with insulin resistance will: 1) Increase insulin sensitivity (assessed by the insulin sensitivity index as derived from glucose and insulin levels obtained during a 2 hour oral glucose tolerance test (OGTT)and insulin growth factor (IGF)-1 levels) 2) Improve cholesterol metabolism (lower LDL, raise HDL and lower triglyceride (TG) levels); and 3) physical activity levels measured by pedometer and 7 day physical activity recall (PAR).
Secondary hypotheses are: Treatment with RSV 5.0 grams daily in individuals with IR will result in: 1)No change in energy intake as measured by food intake by 3 day food diary; 2)No change in body fat mass or distribution (via dual x-ray absorptiometry (DEXA), body mass index (BMI) and waist-to-hip ratio; and 3)Improved Quality of life as assessed by SF-36, compared to PC group.
We will also examine self-reported appetite and satiety as well as biomarkers leptin and adiponectin in the RSV versus PC group. Finally, we will examine the effects of RSV on hepatic (serum Ala aminotransferase, asp aminotransferase, lactate dehydrogenase, alkaline phosphatase, bilirubin, albumin), pancreatic (serum amylase) and renal (BUN and creatinine), function and red blood cell count (CBC with differential) in the IR compared to the PC group.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 0 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Double (Participant, Investigator) |
Primary Purpose: | Treatment |
Official Title: | Mechanisms of Metabolic Regulation of Resveratrol on Humans With Metabolic Syndrome. |
Study Start Date : | May 2007 |
Actual Primary Completion Date : | August 2008 |
Actual Study Completion Date : | August 2008 |

Arm | Intervention/treatment |
---|---|
Placebo Comparator: 2
Placebo
|
Drug: Placebo
Placebo, no active drug, take 5 capsules by mouth daily for one month |
Experimental: Experimental 1
Resveratrol
|
Drug: Resveratrol |
- Insulin sensitivity (assessed by the insulin sensitivity index as derived from glucose and insulin levels obtained during a 2 hour oral glucose tolerance test (OGTT)1, 2 and insulin growth factor (IGF)-1 levels3 [ Time Frame: one month ]
- Improve cholesterol metabolism (lower LDL, raise HDL and lower triglyceride (TG) levels); and 3) physical activity levels measured by pedometer and 7 day physical activity recall (PAR) [ Time Frame: one month ]

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Ages Eligible for Study: | 50 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Adults ages 50 years or older
- Women ages 50 years and older who are postmenopausal, defined as no menses for the previous 12 months
- BMI 25 to 35
- Waist-to-hip circumference ratios for men >0.95, for women >0.85
- HOMA-IR score from fasting plasma glucose and serum insulin levels >2.7
- A diet consisting of > 40% calories from fat; and
- Sedentary, defined as no formal exercise program and less than 30 minutes physical activity weekly.
Exclusion Criteria:
- Active malignancy or tumor or other condition that would severely limit life expectancy
- Any type of major surgery during the last 3 months
- Psychiatric disorders with currently active manifestations
- Insulin-dependent diabetes
- Any chronic medications except for hormone replacement therapy. Vitamin supplements (of any type) are not allowed during the study, but are acceptable if the participant agrees to a 2 week washout period before participation in the study
- Active symptoms suggestive of an acute coronary syndrome or decompensated heart failure
- Currently on low fat diet or special diet (i.e. weight loss)
- Excessive alcohol intake (>3 glasses of wine/1 six pack of beer daily)
- Concurrent participation in any drug studies or studies that require sample of a body fluid (or having finished in the past 6 months)
- Non-English speakers
- Abnormal LFTs.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00654667
United States, California | |
University of California | |
San Francisco, California, United States, 94143-0608 |
Responsible Party: | Marlene Berro, UCSF |
ClinicalTrials.gov Identifier: | NCT00654667 History of Changes |
Other Study ID Numbers: |
CTSI - SOS |
First Posted: | April 9, 2008 Key Record Dates |
Last Update Posted: | March 4, 2015 |
Last Verified: | March 2015 |
Keywords provided by University of California, San Francisco:
Resveratrol Insulin Resistance Metabolic Syndrome Sirtuin 1 |
IGF-1 Satiety Leptin Adiponectin |
Additional relevant MeSH terms:
Resveratrol Metabolic Syndrome X Insulin Resistance Hyperinsulinism Glucose Metabolism Disorders Metabolic Diseases Anti-Inflammatory Agents, Non-Steroidal Analgesics, Non-Narcotic Analgesics Sensory System Agents Peripheral Nervous System Agents Physiological Effects of Drugs |
Anti-Inflammatory Agents Antirheumatic Agents Antineoplastic Agents, Phytogenic Antineoplastic Agents Antioxidants Molecular Mechanisms of Pharmacological Action Protective Agents Enzyme Inhibitors Platelet Aggregation Inhibitors Antimutagenic Agents Anticarcinogenic Agents |