Equivalent Glycemic Load and Insulinemic Response Elicited by 7 Low Carbohydrate Products in Healthy Adults
NCT ID: NCT05870891
Last Updated: 2025-04-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
25 participants
INTERVENTIONAL
2023-06-15
2023-10-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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Peanut Butter Cereal
Consumption of Peanut Butter Cereal
Food
Food
Cinnamon Almond Cereal
Consumption of Cinnamon Almond Cereal
Food
Food
Sriracha Crisps
Consumption of Sriracha Crisps
Food
Food
Cheddar Crisps
Consumption of Cheddar Crisps
Food
Food
Almond Blueberry Butter Bar
Consumption of Almond Blueberry Butter Bar
Food
Food
Peanut Butter and Dark Chocolate Bar
Consumption of Peanut Butter and Dark Chocolate Bar
Food
Food
Almond Dark Chocolate Bar
Consumption of Almond Dark Chocolate Bar
Food
Food
White Bread 5 g available carbohydrate
Consumption of white bread containing 5 g available carbohydrate
Food
Food
White Bread 20 g available carbohydrate
Consumption of white bread containing 20 g available carbohydrate
Food
Food
Interventions
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Food
Food
Eligibility Criteria
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Inclusion Criteria
* Willing to abstain from unusual strenuous exercise and consuming alcoholic drinks for 24 hours before study days
* Willing to refrain from smoking tobacco or marijuana for 12h before and during study visits
* Understanding the study procedures and willing to provide informed consent to participate in the study and authorization to release relevant protected health information to the study investigator
* Subjects must be eligible to receive income in Canada and be covered by a health insurance plan such as OHIP
* Pregnant or lactating individuals
* Personal history of diabetes
* Major trauma or surgical event within 3 months of screening
* The presence of any laboratory result, health condition, illness or drug use that increases risk to the subject or to others or may affect the results, as judged by the Qualified Investigator
* Unwillingness or inability to comply with experimental procedures and to follow INQUIS safety guidelines
* Known intolerance, sensitivity, or allergy to any ingredients in the study test meals. All allergens should be assumed to be a result of manufacturing practices.
* Subject is currently participating or recently (within 30 days of screening) participated in a clinical trial involving long-term exposure (greater than 24 hours) to an investigational drug, nutritional supplement or lifestyle modification
18 Years
75 Years
ALL
Yes
Sponsors
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INQUIS Clinical Research
INDUSTRY
General Mills
INDUSTRY
Responsible Party
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Locations
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INQUIS Clinical Research, Ltd.
Toronto, Ontario, Canada
Countries
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Other Identifiers
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INQ-2324
Identifier Type: -
Identifier Source: org_study_id
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