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
PHASE1
6 participants
INTERVENTIONAL
2015-12-31
2016-07-31
Brief Summary
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Detailed Description
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Several epidemiological studies have suggested that the consumption of anthocyanin-rich foods, including the moderate consumption of red wine, is positively associated with the prevention of cardiovascular heart disease.
It has become clear that the flavonoid bioactive forms in vivo are not necessarily those which occur in nature, but metabolites arising after absorption takes place.Therefore, studying the bioavailability of red wine ANT is very important to identify which metabolites (originated in vivo) can actually reach the target organs (and in which concentrations) and may be responsible for the postulated health benefits of red wine.
Intervention protocol:
Urine samples and peripheral venous blood (10 ml) will be collected from 10 h-fasting subjects. Afterwards, each volunteer will consume 250 ml of table red wine or 150 ml of young Port red wine and blood samples will be collected 15, 30, 60 and 120 min after wines ingestion. Another urine sample will be collected at 120 min.
Table red wine 12 % (250 ml) and young Port red wine 20 % (150 ml), two different food matrices rich in ANT, provided the same amount of ethanol (24 g of ethanol).
A thorough screening analysis for ANT will be performed in plasma and urine samples collected from the volunteers at different time points.
Conditions
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Keywords
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Study Design
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CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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Table Red Wine
250 ml Table Red Wine (12% ethanol)
Table Red Wine
Young Port Red Wine
150 ml Young Port Red Wine (20% ethanol)
Young Port Red Wine
Interventions
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Table Red Wine
Young Port Red Wine
Eligibility Criteria
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Inclusion Criteria
* Age 18-65 years
* BMI \< 25 kg/m2
* Willing and able to provide written consent
Exclusion Criteria
* Subjects under prescription of any chronic medication
* Intake of red fruits or red wine in the last 24 h prior to the beginning of the intervention
* Subjects involved in any clinical or food study within the preceding month
18 Years
45 Years
MALE
Yes
Sponsors
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REQUIMTE/LAQV, Departamento de Química e Bioquímica, FCUP
UNKNOWN
Center for Health Technology and Services Research
OTHER
Vinoflavo
INDUSTRY
Universidade do Porto
OTHER
Responsible Party
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Principal Investigators
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Conceição Calhau, PhD
Role: PRINCIPAL_INVESTIGATOR
CINTESIS - Faculty of Medicine of University of Porto
Locations
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CINTESIS - Faculty of Medicine of the University of Porto
Porto, , Portugal
Countries
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Other Identifiers
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VINOFLAVO_02
Identifier Type: -
Identifier Source: org_study_id