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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03192605
Other study ID # UPEI
Secondary ID
Status Completed
Phase N/A
First received June 16, 2017
Last updated June 19, 2017
Start date May 15, 2017
Est. completion date June 2, 2017

Study information

Verified date June 2017
Source University of Prince Edward Island
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of the study is to determine how wild blueberry consumption affects glucose regulation, gastrointestinal hormones and satiety in healthy adults.


Description:

Healthy men and women (ages 21 - 65 years) were recruited to take part in a randomized, placebo controlled crossover design study. Subjects were screened to determine their health status (e.g. height, weight, body mass index, blood pressure and medical history). Subjects were randomly assigned to a sequence of two treatments with two study periods. The treatments are frozen wild blueberries and a placebo developed to match calories and fiber of the frozen wild blueberries. The subjects were asked to avoid high polyphenol foods in their typical diet for 7 days and consume one of the two treatments as a dietary intervention. After the seventh day subjects consumed a test meal along with either the wild blueberry or placebo. Blood was collected to determine glucose and satiety hormone levels.


Recruitment information / eligibility

Status Completed
Enrollment 17
Est. completion date June 2, 2017
Est. primary completion date June 2, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 65 Years
Eligibility Inclusion Criteria:

- Male or female

Exclusion Criteria:

- BMI < 20 and > 30 kg/m²

- Pregnant women or women who plan on becoming pregnant during the study

- Postpartum women

- Lactating women

- Diabetes Mellitus

- Kidney disease

- Liver disease

- GI Disease

- Certain cancers

- Smokers

- Blueberry allergies

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Blueberry
Blueberry - 150 grams wild blueberries (whole fruit)
Placebo
Placebo - matched for calories and fiber

Locations

Country Name City State
Canada University of Prince Edward Island, Health Sciences Charlottetown Prince Edward Island

Sponsors (1)

Lead Sponsor Collaborator
University of Prince Edward Island

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Glucose (mmol/L) Plasma glucose Change from baseline 0 hours and 2 hours
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