Skip to content

The effects of resveratrol on serum apolipoprotein A-I concentrations in men and women with low HDL-cholesterol concentrations.

The effects of resveratrol on serum apolipoprotein A-I concentrations in men and women with low HDL-cholesterol concentrations. - Resveratrol and serum apo A-I

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON38326
Enrollment
50
Registered
2010-11-15
Start date
2011-05-10
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

a low concentration of the protective ('good') cholesterol Low HDL cholesterol

Interventions

During the experimental period, subjects will receive one capsule at lunch and one at dinner daily. Each capsule will provide 75 mg resveratrol. During the control period, subjects will receive two

Sponsors

Medisch Universitair Ziekenhuis Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • aged between 45 and 70 years • HDL-C

Exclusion criteria

Exclusion criteria: • unstable body weight (weight gain or loss >3 kg in the past 3 months) • indication for treatment with cholesterol-lowering drugs according to the Dutch Cholesterol Consensus • use of medication or a medically-prescribed diet known to affect serum lipid or glucose metabolism. Oral anti-contraceptives and paracetamol are allowed. • Active cardiovascular disease (for instance congestive heart failure) or recent (21 glasses of alcohol-containing drinks per week women: consumption of >14 glasses of alcohol-containing drinks per week • abuse of drugs • pregnant or breastfeeding women • participation in another biomedical study within 1 month prior to the screening visit • having donated blood (as blood donor) within 1 month prior to the screening visit or planning to do so during the study • impossible or difficult to puncture as evidenced during the screening visits

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the change in serum apoA-I concentrations and serum HDL-C.

Secondary

MeasureTime frame
-flow-mediated dilation -pulse wave velocity -glucose- en insulineconcentration -ApoB -Total cholesterol -LDL-C -Triglycerides -hdCRP -IL-6 -sICAM-1 -VCAM-1 -MCP-1 -sE Selectin - Blood chemistry: phosphorus, sodium, potassium, chloride, calcium, creatinine, blood urea nitrogen (BUN), protein, albumin, gammaGT, aspartate-aminotransferase (AST), alanine-aminotransferase (ALT), alkaline phosphatase (ALP), bilirubin - Haematology: White cell count, red cell count, platelet count, hemoglobin, hematocrit, mean cell volume, and mean cell hemoglobin concentration, red cell distribution - Blood coagulation: Prothrombin time (PT) and aPT

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)