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

Last updated: January 8, 2025
Sponsor: TCI Co., Ltd.
Overall Status: Active - Recruiting

Phase

N/A

Condition

Vascular Diseases

Treatment

Buckwheat husk extract

Placebo

Clinical Study ID

NCT04490720
201911003RSC
  • Ages 20-65
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

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

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. 20 to 65-year-old males or non-pregnant females who are willing to sign thesubject's consent.

  2. The systolic blood pressure is 121-139 mmHg and the diastolic blood pressure isbetween 81-89 mmHg.

  3. Those who are not pregnant and are willing to cooperate with contraception duringthe trial period.

  4. No history of organ transplantation, epilepsy or convulsions, liver or kidneydisease, malignant tumor, endocrine disease, mental disease, alcohol or drug abuse,or other major organic diseases (according to medical history).

Exclusion

Exclusion Criteria:

  1. Pregnant women.

  2. People with a history of organ transplantation, epilepsy or convulsions, liver andkidney disease, malignant tumors, endocrine diseases, mental illness, alcohol ordrug abuse, and other major organic diseases (according to medical history).

  3. No person has undergone major surgery.

Study Design

Total Participants: 60
Treatment Group(s): 2
Primary Treatment: Buckwheat husk extract
Phase:
Study Start date:
November 24, 2021
Estimated Completion Date:
February 28, 2026

Study 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.

Connect with a study center

  • National Taiwan University Hospital

    Taipei, 114
    Taiwan

    Active - Recruiting

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