- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02005796
Bioavailability of Anthocyanins of Blue Potatoes as Compared With Bilberries
May 19, 2015 updated by: Kaisa Linderborg, University of Turku
In this study, the postprandial glycemia and insulinemia caused by boiled potato with blue-fleshed or yellow-fleshed tubers, or a gel prepared with bilberries and potato starch, is studied in healthy males.
Additionally, the appearance and metabolism of the flavonoids and their metabolites is studied in plasma and urine.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
14
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Turku
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University of Turku, Turku, Finland, 20014
- Department of Biochemistry, University of Turku
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 45 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Age 18-45
- Male
- No regular medication
- No participation in a drug trial or blood donation within 2 months
- Non-smoker
- Signs informed consent
- Body mass index 18.5-27 kg/m2
- Fasting plasma cholesterol < 5.5 mmol/l
- Fasting plasma triacylglycerols < 2.6 mmol/l
- Fasting plasma glucose 4-6 mmol/l
- blood pressure <140/80 mmHg
- hemoglobin>130 g/l
- Fasting plasma alanine amino transferase (ALAT) <60 U/l (normal liver function)
- Fasting plasma thyroid-stimulating hormone (TSH) 0.4 - 4.5 mU/l (normal thyroid function)
- Fasting plasma creatinine <118 µmol/l (normal kidney function)
Exclusion Criteria:
- Regular smoking
- Alcohol abuse
- Regular medication
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Blue-fleshed potato tubers
Intervention: Steam cooked mashed potato tubers
|
|
|
Experimental: Yellow-fleshed potato tubers
Intervention: Steam cooked mashed potato tubers
|
|
|
Experimental: Bilberries and potato starch
Intervention: A gel boiled with bilberries and potato starch
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Plasma glucose concentration
Time Frame: 20min, 40min, 60min, 90min, 120min, 180min, 240min
|
20min, 40min, 60min, 90min, 120min, 180min, 240min
|
|
Plasma insulin concentration
Time Frame: 20min, 40min, 60min, 90min, 120min, 180min, 240min
|
20min, 40min, 60min, 90min, 120min, 180min, 240min
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Concentrations and quality of flavonoid color compounds or their metabolites in plasma and urine (HPLC-measurement)
Time Frame: 20min, 40min, 60min, 90min, 120min, 180min, 240min
|
20min, 40min, 60min, 90min, 120min, 180min, 240min
|
|
Concentrations and quality of flavonoid color compounds or their metabolites in plasma and urine (NMR-measurement)
Time Frame: 20min, 40min, 60min, 90min, 120min, 180min, 240min
|
20min, 40min, 60min, 90min, 120min, 180min, 240min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2013
Primary Completion (Actual)
May 1, 2015
Study Completion (Actual)
May 1, 2015
Study Registration Dates
First Submitted
December 3, 2013
First Submitted That Met QC Criteria
December 3, 2013
First Posted (Estimate)
December 9, 2013
Study Record Updates
Last Update Posted (Estimate)
May 20, 2015
Last Update Submitted That Met QC Criteria
May 19, 2015
Last Verified
May 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- Siniset perunat
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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