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Trials / Recruiting

RecruitingNCT04490720

The Efficacy Evaluation of Buckwheat Husk Extract on Cardiovascular Disease Risk Factors

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
TCI Co., Ltd. · Industry
Sex
All
Age
20 Years – 65 Years
Healthy volunteers
Accepted

Summary

To assess the efficacy evaluation of buckwheat husk extract on cardiovascular disease risk factors

Detailed description

This is a double-blind and randomized study. Subjects are informed to consume the samples every day for 2 months. The clinical diagnosis item of cardiovascular disease is evaluated by the doctor.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPlaceboconsume 1 sachet per day for 2 months
DIETARY_SUPPLEMENTBuckwheat husk extractconsume 1 sachet per day for 2 months

Timeline

Start date
2021-11-24
Primary completion
2025-12-31
Completion
2026-02-28
First posted
2020-07-29
Last updated
2025-01-09

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT04490720. Inclusion in this directory is not an endorsement.

The Efficacy Evaluation of Buckwheat Husk Extract on Cardiovascular Disease Risk Factors (NCT04490720) · Clinical Trials Directory