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Completed

NCT Number: NCT00869193

Effect of Grape Seed Extract on Blood Pressure

The purpose of this study is to determine whether an 8-week intervention with grape seed extract is effective in reducing daytime ambulatory blood pressure in male and postmenopausal female with elevated daytime blood pressure values.

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Key information

Age range

35 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Unilever R&D Vlaardingen

Vlaardingen, 3133 AT, Netherlands

About this study

Background: High blood pressure is a major risk factor for morbidity and mortality from stroke, heart disease, and end-stage renal disease. Several studies have shown that dietary polyphenols derived from fruits and vegetables (including those from grape products) can lower blood pressure in both normotensive and hypertensive subjects.

Study objectives: Primary objective: To study, in subjects with elevated blood pressure levels, the effects of grape seed extract high in polyphenols, on daytime ambulatory systolic and diastolic blood pressure (SBP and DBP, respectively). Secondary objective: To explore mechanistic pathways responsible for the blood pressure lowering efficacy in case a blood pressure lowering effect is shown.

Study population: Each treatment group will consist of 35 men and postmenopausal women (35-75 years of age) with daytime SBP between 120 and 159 mmHg. The total number of subjects will be 70.

Study design: This study will have a randomized, double-blind, placebo-controlled parallel design with 2 treatments, a 1-week run-in period, and an 8-week intervention period. The 2 treatments will consist of placebo capsules and capsules with grape seed extract.

Study outcomes: Daytime ambulatory blood pressure (ABP) will be measured every 20 minutes for 2 x 12 hours at baseline and 2 x 12 hours at the end of intervention. Furthermore, before and after the intervention period, 24-hour urine will be collected and 2 blood samples will be taken in order to investigate mechanistic pathways and platelet function.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and postmenopausal female subjects in the age ≥ 35 and ≤ 75 at start of the study
  • BMI ≥ 18.5 and ≤ 30.0 kg/m2
  • Apparently healthy: no reported diseases that may affect study results and pre-selected blood parameters within normal range
  • Informed consent signed
  • Willing to refrain from supplements, food products, diets and drugs that may interfere with the outcomes of the study

Exclusion criteria

  • Mean of 6-hour ambulatory SBP < 120 mmHg, > 159 mmHg and/or DBP > 99 mmHg
  • 10-year risk mortality risk on CVD > 10% according to NHG standard M84. For subjects > 65 years of age and SBP ≥ 140 mmHg the study physician will assess eligibility
  • Irregular pulse or pulse < 50 or > 100 bpm
  • Intense exercise >10 h/w
  • Reported weight loss/gain > 10% of body weight in the 6 month preceding pre-study examination
  • The habit of smoking during the past year

Treatment and study plan

Grape seed extract

Dietary Supplement

Subjects will daily consume one capsule with grape seed extract for 8 weeks.

Other names: Polyphenol

Microcrystalline Cellulose (placebo)

Dietary Supplement

Subjects will daily consume one capsule with microcrystalline cellulose for 8 weeks.

Primary outcomes

  1. Difference between treatment and placebo in changes from baseline of ambulatory systolic and diastolic blood pressure

    Time frame: 8 weeks of intervention

Secondary outcomes

  1. Difference between treatment and placebo in changes from baseline of mechanistic markers in plasma and/or urine (vasoactive factors and markers of polyphenol metabolism) and platelet function (only measured in case of a relevant BP-lowering effect)

    Time frame: 8 weeks of intervention

Sponsors and collaborators

Lead sponsor

Unilever R&D

Industry

Collaborators

  • University of Edinburgh

Registry information

Official study title

Effect of Grape Seed Extract High in Polyphenols on Blood Pressure in Subjects With Elevated Blood Pressure Levels

Important dates

Study start
2009
Primary completion
2009
Study completion
2009
First posted
Mar 25, 2009
Registry last updated
Aug 28, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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