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WithdrawnNCT00654667RSVUpdated Mar 4, 2015

Mechanisms of Metabolic Regulation of Resveratrol on Humans With Metabolic Syndrome

A Phase 2 interventional study of Placebo and Resveratrol in Insulin Resistance, sponsored by University of California, San Francisco. Withdrawn at 1 site in United States. Open to participants aged 50 Years and older. Per ClinicalTrials.gov, last updated 2015-03-04.

Sponsored by University of California, San Francisco · Phase 2, Interventional, and Treatment

Why this study was withdrawn
no participant enrollment
Phase
Phase 2
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
50 Years and older
Sex
All
01

Study summary

Sirtuin activators may prove useful in treating age-related diseases and extending lifespan in humans. Resveratrol (RSV), a polyphenol found in red wine, has been shown in vitro to enhance SIRT1 activity. RSV is associated with some of the beneficial effects of red wine or the "French Paradox". Recently RSV has been associated with increasing lifespan in mice on a high calorie diet and improved metabolic profile and activity levels. The effect of this small molecule in humans is unknown. Preclinical observations suggest that RSV is safe and has enormous potential in the treatment of obesity and insulin resistance in humans. This pilot study will examine the effect of RSV on improving the metabolic profile of adults with insulin resistance. Specifically, this randomized double blind placebo controlled study will examine the effects of 4 weeks of supplementation with RSV 5.0 grams daily, compared to placebo control (PC) on the metabolic profile of 36 men and women over the age of 50 with insulin resistance (IR) consuming a typical western diet consisting of at least 40% calories from fat.

Read the detailed description

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.

02

Conditions studied

  • Insulin Resistance

Keywords

  • Resveratrol
  • Insulin Resistance
  • Metabolic Syndrome
  • Sirtuin 1
  • IGF-1
  • Satiety
  • Leptin
  • Adiponectin
03

In context

Metabolic Syndrome

1,964 studies on the registry are indexed under Metabolic Syndrome; 330 are open to participants now.

Browse Metabolic Syndrome studies →

Lead sponsor

University of California, San Francisco is the lead sponsor of 2,132 studies on the registry; 375 are open to participants now.

Of its 262 completed or terminated interventional studies of FDA-regulated products, 196 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Adults ages 50 years or older
  2. Women ages 50 years and older who are postmenopausal, defined as no menses for the previous 12 months
  3. BMI 25 to 35
  4. Waist-to-hip circumference ratios for men >0.95, for women >0.85
  5. HOMA-IR score from fasting plasma glucose and serum insulin levels >2.7
  6. A diet consisting of > 40% calories from fat; and
  7. Sedentary, defined as no formal exercise program and less than 30 minutes physical activity weekly.

Exclusion criteria

Exclusion Criteria:

  1. Active malignancy or tumor or other condition that would severely limit life expectancy
  2. Any type of major surgery during the last 3 months
  3. Psychiatric disorders with currently active manifestations
  4. Insulin-dependent diabetes
  5. 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
  6. Active symptoms suggestive of an acute coronary syndrome or decompensated heart failure
  7. Currently on low fat diet or special diet (i.e. weight loss)
  8. Excessive alcohol intake (>3 glasses of wine/1 six pack of beer daily)
  9. Concurrent participation in any drug studies or studies that require sample of a body fluid (or having finished in the past 6 months)
  10. Non-English speakers
  11. Abnormal LFTs.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
0 participants (actual)

Study arms

  • Placebo comparator
    2

    Placebo

    Drug: Placebo

  • Experimental
    Experimental 1

    Resveratrol

    Drug: Resveratrol

Interventions

  • DrugPlacebo

    Placebo, no active drug, take 5 capsules by mouth daily for one month

  • DrugResveratrol
06

What researchers measure

Primary outcomes

  1. 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

Secondary outcomes

  1. 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

07

Study locations

1 site
  • University of California
    San Francisco, California 94143-0608, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 4, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00654667
Lead sponsor
University of California, San Francisco
First posted
Apr 9, 2008
Start date
May 2007
Primary completion
Aug 2008
Completion
Aug 2008
Last update
Mar 4, 2015

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is withdrawn, as verified in Mar 2015. You cannot join it, but the record below documents what was studied.

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