Clinical Trials Directory

Trials / Completed

CompletedNCT03211767

Double-Blind, Randomized, Cross-Over Trial of Aged Garlic Extract for Hypertension

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
43 (actual)
Sponsor
University of Manitoba · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this trial is to assess the effect of consumption of aged garlic extract powder on 24 h systolic and diastolic ambulatory blood pressure in hypertensive individuals following 8 weeks of supplementation. Additional secondary objectives are to assess the effects of aged garlic extract powder intake for 8 weeks on lipid profile (TC, HDL-C, LDL-C, and TG concentrations), blood glucose, office blood pressure, pulse-wave velocity and augmentation index, body mass index, and waist and hip circumference.

Detailed description

Forty hypertensive volunteers between 18 and 75 years will be recruited from the Winnipeg (Manitoba, Canada) area to participate in a two arm crossover, double-blind, randomized, placebo-controlled intervention study for 8 weeks per study period following obtainment of informed consent. The 2 periods of treatment will include: 1. Treatment period: One capsule twice a day, providing 600 mg each of aged garlic extract powder, for a total of 1200 mg/day of aged garlic extract powder. 2. Control period: The control product will be an identical-looking placebo capsules containing cellulose, which is being used as a filler in the treatment capsules.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTAged garlic extractEach capsule contains 600mg of aged garlic extract powder
DIETARY_SUPPLEMENTPlaceboEach capsule contains cellulose as a filler.

Timeline

Start date
2017-10-12
Primary completion
2018-07-25
Completion
2018-07-25
First posted
2017-07-07
Last updated
2019-02-12

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03211767. Inclusion in this directory is not an endorsement.