Clinical trial Recruiting at 1 site Interventional Ages 20 to 40

Investigating the cardiovascular benefits of wild rice consumption

Official title: A Multidisciplinary Investigation of Cardiovascular Benefits of Wild Rice

Run by University of Manitoba · NCT04119791 · Data updated 2026-11-12

This study is testing whether eating wild rice every day for a month can improve heart health in healthy adults.

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Quick facts

Study typeInterventional
Ages20 Years to 40 Years
SexAll
Enrollment48 (estimated)
SponsorUniversity of Manitoba
Academic / other
Locations1 site (Winnipeg, Manitoba)
StatusRecruiting
StartedNovember 5, 2024
Main results expectedJanuary 30, 2026
Study endsJanuary 30, 2028
Registry record updatedMarch 3, 2025
Trial IDNCT04119791 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are healthy adults aged 20 to 40 years, both male and female.

Probably not a fit

Patients who are pregnant, lactating, smokers, obese, or on medications for cardiovascular, diabetes, or cancer diseases may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study involves 24 healthy adult males and females who will consume approximately 30 grams of wild rice daily for 28 days. The primary aim is to assess the impact of wild rice on cardiovascular risk factors before and after the intervention. The study is designed as a pilot to explore the potential health benefits of wild rice, which has not been previously tested in clinical trials. The research is conducted by the Department of Food and Human Nutritional Sciences at the University of Manitoba, known for its contributions to food and nutrition research.

Why it matters

Potential benefit: If successful, this study could provide insights into dietary interventions that may reduce cardiovascular risk factors.

How similar studies have gone: While the effects of wild rice have not been tested in clinical trials, other studies on functional foods have shown promising results in improving health outcomes.

Who can join: the full rules

Show full inclusion / exclusion criteria
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

Where it's running

  • St. Boniface Hospital Research Center Asper clinical
    Winnipeg, Manitoba, Canada
    Recruiting

Study contacts

  • Principal investigator: Mohammed H Moghadasian, PhD — University of Manitoba
  • Study coordinator: Mohammed H Moghadasian, PhD
  • Email: mmoghadasian@sbrc.ca
  • Phone: 204-235-3934

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.