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Dietary polyphenols as modulators of lipid oxidation and mitochondrial function in overweight volunteers

Dietary polyphenols as modulators of lipid oxidation and mitochondrial function in overweight volunteers - Polyphenols and fat oxidation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON38206
Enrollment
60
Registered
2010-10-26
Start date
2011-03-23
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

impaired fat oxidation overweight

Interventions

3 different dietary polyphenol conditions: A. EGCG (282mg daily) + resveratrol (200mg daily) B. EGCG (282mg daily) + resveratrol (200mg daily) + soy isoflavones (48mg genistein daily) C. Placebo

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Overweight men and women (BMI>=25kg/m2- 34.9kg/m2), - Aged 20-35 and 35-50 years - Caucasian - Normal fasting glucose (

Exclusion criteria

Exclusion criteria: - Women lactating, pregnant or (post) menopausal - Regular smokers - People with intensive fitness training, eg. athletes (>= 3 per week >= 1 hour training) - Habitual consumption of green tea (more than 1 cup per day) or products containing green tea extract - Total caffeine consumption > 300 mg/day (1 can of cola or 2 cups of regular coffee or 2 cups of black tea or 1 cup of coffee and 1 cup of black tea or other combinations) - Alcohol intake >20 g/day (2 glasses of beer or wine) - Any dietary vitamins or dietary supplements - Diabetes mellitus (defined as FPG >= 7.0 mmol/l and/or 2hPG >= 11.1 mmol/l) - Serious pulmonary, cardiovascular, hepatic or renal disease - History of cardiovascular disease - All other relevant medical disorders that potentially interfere with this trial (e.g. history of gastro-intestinal, liver or thyroid disorders) - Current use of medication interfering with study intervention or interfering with study endpoints/hypotheses (e.g. medication containing caffeine like analgesics, anorectics and analeptics) - Not to be able to understand the study information - Subjects on a special diet or vegetarian - Blood donation 2 months prior to the study and during the study - Participation in other studies - Drug use - Use of anti-coagulant medication

Design outcomes

Primary

MeasureTime frame
The primary study parameter is the difference in postprandial fat oxidation after the 3 polyphenol conditions

Secondary

MeasureTime frame
As secondary endpoints, differences in the systemic and local tissue lipolysis, mitochondrial function, oxidative stress, insulin sensitivity and body composition between the various polyphenol supplements are examined.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)