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Clinical Trials in Canada / NCT04119791
Recruiting Not applicable

A Multidisciplinary Investigation of Cardiovascular Benefits of Wild Rice

NCT04119791 · tracked via the Priya Life Science Canada tracker
Sponsor
University of Manitoba
Phase
Not applicable
Started
2024-11-05
Last updated
2025-03-03

Condition(s) studied

Healthy DietHealthy

Investigational drug(s) / intervention(s)

wild rice

wild rice: 30 grams of wild rice in the form salad, snack bar and soup

Study summary

In this study 24 adult males and adult females, with overall healthy condition, will consume approximately 30 grams of wild rice every day for 28 days. Cardiovascular risk factors will be assessed at the beginning and at the end of the study.

Eligibility

Sex
ALL
Min age
20 Years
Max age
40 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Male * Female * Both genders are healthy * 20 - 40 years old Exclusion Criteria: * Non-pregnant * Non-lactating * Non-smokers * Not obese (Body Mass Index (BMI) \< 30) * Not currently on any medications for cardiovascular, diabetes, and cancer diseases

Primary outcome measure(s)

  • Wild rice alters gut microbiome. — 4 weeks
    This study is designed to investigate the effects of wild rice consumption on gut microbiome diversity and population in volunteer healthy young adults.
  • Changes in gut microbiome alters macronutrient metabolism. — 4 weeks
    In this study, the investigators will establish whether changes in gut microbiome due to consumption of wild rice may result in altered macronutrient metabolism by studying plasma metabolomics.

Trial sites (1)

FacilityCityRegionStatus
St. Boniface Hospital Research Center Asper clinical Winnipeg Manitoba Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04119791 on ClinicalTrials.gov ↗ ← All trials in Canada