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The Effect of Black Currant on Postprandial Glucose Metabolism

The Effect of Black Currant on Postprandial Glucose Metabolism

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04150926
Acronym
MAQUA
Enrollment
26
Registered
2019-11-05
Start date
2019-08-15
Completion date
2020-04-30
Last updated
2020-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postprandial Hyperglycemia, Prediabetic State

Keywords

berries, black currant, glucose, glycemia, quinoa

Brief summary

The study examines the effect of black currant on glucose and insulin concentrations after a meal. In addition, the cytokine and free fatty acids levels are of interest.

Detailed description

The study examines the effect of black currant on glucose and insulin concentrations after a meal. Healthy (n= 30) volunteers are recruited to participate in four consecutive visits in the research laboratory, when four meals are served in randomised order. Meals are: black currant puree, black currant and quinoa based snack, quinoa base and liquid containing glucose, fructose and sucrose. The meals contain the same amount of carbohydrates. In addition to glucose and insulin concentration, cytokine and free fatty acid concentrations are measured after each meal.

Interventions

OTHERBlack currant

The effect of black currant puree will be compared with black currant-quinoa product, quinoa base and with liquid with glucose, fructose and sucrose Experimental: Black currant and quinoa product Active Comparator: Quinoa base Meal study comparing the effect of black currant puree with liquid with glucose, fructose and sucrose, black currant and quinoa product and quinoa base

OTHERBlack currant-quinoa product

The effect of black currant puree will be compared with black currant-quinoa product

OTHERQuinoa base

The effect of black currant puree will be compared with quinoa base

Sponsors

Savonia University of Applied Sciences
CollaboratorOTHER
Regional Development Company SavoGrow
CollaboratorUNKNOWN
University of Eastern Finland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Masking description

Products are visibly differing from each other.

Intervention model description

Meal studies in randomised order

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* age: 25-65 years * BMI: 20-28 kg/m2 * Perceived health status: Good

Exclusion criteria

* fasting glucose: \> 7.0 mmol/l * LDL-cholesterol: \> 3.0 mmol/l * total cholesterol: \> 6.5 mmol/l * blood pressure : \> 160/100 mmHg * weight change of \> 5% during previous 6 months or active weightreduction * no serious chronic diseases * one exception of the

Design outcomes

Primary

MeasureTime frameDescription
Glucose concentration0 minutes until 180 minutesGlucose concentration after meal
Insulin concentration0 minutes until 180 minutesInsulin concentration after meal

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026