Study on the Effects of Epicatechin and Quercetin Supplementation on Vascular Function and Blood Pressure (FLAVO)

W

Wageningen University

Status

Completed

Conditions

Hypertension
Endothelial Dysfunction

Treatments

Dietary Supplement: Quercetin
Dietary Supplement: Placebo
Dietary Supplement: Epicatechin

Study type

Interventional

Funder types

Other

Identifiers

NCT01691404
NL4077208112

Details and patient eligibility

About

Flavonoid-rich foods such as tea and cocoa have been identified as having a blood pressure-lowering effect. Part of this effect is thought to be due to the flavonoid content of these foods although it is currently unknown which flavonoids play a role. Epicatechin is one the major flavonoids in cocoa while quercetin is largely found in tea. During this study the investigators plan to investigate the effects of pure epicatechin and quercetin supplementation on vascular function and blood pressure in untreated (prehypertensive) subjects by way of a three-armed double-blind crossover intervention. Participants will sequentially consume supplements containing quercetin, epicatechin or placebo for a period of 4 weeks. Before and after this 4 week period, measurements of vascular function and blood pressure will be taken. The investigators hypothesize that the supplementation of epicatechin and quercetin will improve vascular function and blood pressure.

Full description

By means of a three-armed double-blind crossover intervention, the effects of pure flavonoid supplementation will be investigated. The products under investigation will be epicatechin and quercetin-3-glucoside. Subjects will be asked to consume either 160mg of quercetin-3-glucoside, 100mg of epicatechin or a placebo capsule for a period of 4 weeks. Measurements of vascular function and blood pressure will be taken before and after each 4-week intervention period. A 4-week washout period will be planned between each intervention. Measurements of vascular function will include flow-mediated dilation, pulse wave analysis, pulse wave velocity and vasomotion as well as biomarkers of inflammation and vascular function.

Enrollment

38 patients

Sex

All

Ages

30 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Systolic Blood Pressure between 125 and 160 mmHg
  • Age between 30 and 80 years
  • BMI > 20 and ≤ 40
  • No reported current or previous metabolic diseases
  • No history of cardiovascular diseases
  • No history of renal, liver or thyroid diseases
  • No history of gastrointestinal diseases
  • No diabetes mellitus
  • Fasting laboratory parameters within normal range: complete blood count (RBC, WBC, PLT, HB, HT), renal function (serum creatinine, urea), liver function (ALAT, ASAT, ɣ-GT), and serum glucose.

Exclusion criteria

  • Body mass index > 40 and ≤20
  • Secondary hypertension
  • Weight loss or weight gain of 5 kg or more during the last 2 months
  • Usage of non-steroidal anti-inflammatory drugs (acetylsalicylic acid, ibuprofen, naproxen) and not able or willing to stop taking them from at least 4 weeks prior to the study
  • Usage of cholesterol-lowering medication
  • Daily usage of corticosteroids
  • Medical treatment that may affect blood pressure and not able (or willing) to stop
  • Taking nutritional supplements and unwilling to discontinue
  • Lactating, pregnant or intention to become pregnant during study
  • Reported dietary habits, medically prescribed diet, slimming diet
  • Reported average alcohol consumption > 2 glasses/d (men) or >1 glass/d (women)
  • Problems with consuming the supplements or following the study guidelines
  • Unwilling to undergo home or office blood pressure measurements
  • Recent blood donation i.e. 1 month (male subjects) or 2 months (female subjects) prior to the study and planned donation during the study period
  • Reported intense sporting activities > 10 h/w
  • Not agreeing to be informed about unexpected and medically relevant personal test-results, or not agreeing that their general practitioner will be informed about these results
  • Participation in another biomedical trial less than 2 months before the start of the study or at the same time
  • No signed informed consent form
  • Clinical disorders that could interfere with the intervention
  • Unable to comply with the study procedure (e.g. holidays, urine collection, blood sampling)
  • Smokers
  • Difficulty imaging brachial artery by ultrasonography

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

38 participants in 3 patient groups, including a placebo group

Epicatechin
Active Comparator group
Description:
Subjects will be asked to consume supplements containing 100mg of epicatechin daily
Treatment:
Dietary Supplement: Epicatechin
Quercetin
Active Comparator group
Description:
Subjects will be asked to consume supplements containing 160mg of quercetin-3-glucoside daily
Treatment:
Dietary Supplement: Quercetin
Placebo
Placebo Comparator group
Description:
Subjects will be asked to consume capsules containing a placebo (cellulose) daily
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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