Skip to main content
OpenTrials
Completed

NCT Number: NCT02326766

Blood Pressure Lowering Effect of Supplementation With Korea Red Ginseng Associated With Reductions in Circulating Lp-PLA2 Activity and Lysophospatidylcholines and an Increase in Dihydrobiopterin in Prehypertensive Subjects

This study evaluated effects of red ginseng consumption on blood pressure (BP) and fasting plasma metabolomes.

Completed

Looking for future studies?

Notify Me

Key information

Age range

20 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

About this study

A randomized, double-blind, placebo-controlled study was conducted on nonobese, nondiabetic and prehypertensive subjects. Over a 12 week test period, the red ginseng group (n=31) consumed 10 capsules (total 5g) daily containing red ginseng, while the placebo group (n=31) consumed the same product without red ginseng. Fasting plasma metabolomes were profiled using UPLC-LTQ-Orbitrap mass spectrometry.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • nondiabetic, nonobese and prehypertensive subjects with blood pressures ranging 120 - 139 mmHg (systolic) or 80-89 mmHg (diastolic) were enrolled in this study.

Exclusion criteria

  • exclusion criteria included previous diagnosed clinical hypertension
  • self-reported use of antihypertensive medication
  • abnormal liver or renal function
  • history of cardiovascular disease
  • kidney disease
  • cancer
  • thyroid or pituitary disease or any other serious life-threatening illness that required regular medical treatment
  • we also excluded women who were pregnant, breast feeding or intending to become pregnant during the time of study.

Treatment and study plan

KRG

Dietary Supplement

5g Korea red ginseng (KRG)

Placebo

Dietary Supplement

5g placebo

Primary outcomes

  1. changes from baselilne in blood pressure

    Time frame: 12 week

Secondary outcomes

  1. changes from baseline in plasma metabolites

    Time frame: 12 week

Sponsors and collaborators

Lead sponsor

Yonsei University

Other

Registry information

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Dec 29, 2014
Registry last updated
Dec 29, 2014

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.

Published trials that share one or more normalized conditions with this study.