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Anthocyanin-rich Blackcurrant and Vascular Function

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University of Reading

Status

Completed

Conditions

Inflammation
Vascular Stiffness

Treatments

Other: Beverage: Placebo (sucrose, glucose, fructose, maltodextrin, malic acid, citric acid, vitamin C, artificial blackcurrant flavouring and low-nitrate water)
Other: Beverage: Spray dried blackcurrant powder dissolved in water

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02459756
UREC 14/17

Details and patient eligibility

About

Regular consumption of fruits and vegetables may improve human health and reduce the risk of chronic diseases, such as heart disease, certain cancers and type 2 diabetes, but the active components and the underlying mechanisms are poorly understood. Berry fruits are abundant in anthocyanins and this study aims to test the hypothesis that ingestion of an anthocyanin-rich blackcurrant beverage will improve markers of cardiovascular health (health of blood vessels, inflammation and platelet function). Further, the study will investigate the anthocyanin bioavailability from the blackcurrant beverage.

Enrollment

23 patients

Sex

All

Ages

30 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Aged 30-55 years
  • Non-smoker
  • BMI between 20 - 30 kg/m2
  • Generally healthy as established by a 'health and lifestyle' questionnaire and a screening blood sample
  • Blood pressure < 140/90mmHg
  • Total cholesterol < 6.2 mmol/L
  • Fasting glucose < 7.0 mmol/L

Exclusion criteria

  • Diabetes mellitus
  • Heart problems, stroke, vascular disease
  • Inflammatory disease
  • Kidney, liver, pancreas or gastrointestinal diseases
  • Medication for hyperlipidaemia, hypertension, hypercoagulation, inflammatory conditions
  • Asthma
  • Allergies
  • Smokers (social smokers who agree to abstain for 1 month before and during the study not excluded)
  • Taking phytochemical, antioxidant or fish oil supplements (unless willing to stop for the study period)
  • Taking aspirin > 2 times per month and unwilling to abstain from aspirin ingestion for 14 days prior each study visit
  • History of alcohol misuse
  • Consumption of alcohol >21 units (men) or >15 units (women)
  • Vegans
  • Intense aerobic exercise >20 min 3 x per week
  • Participation in another clinical trial
  • Antibiotics in previous 3 months before study
  • Low haemoglobin levels
  • Females who are pregnant, lactating, or if of reproductive age and not using a reliable form of contraception (including abstinence)

Trial design

23 participants in 2 patient groups, including a placebo group

Intervention
Active Comparator group
Description:
Spray dried blackcurrant powder dissolved in water
Treatment:
Other: Beverage: Spray dried blackcurrant powder dissolved in water
Placebo
Placebo Comparator group
Description:
(sucrose, glucose, fructose, maltodextrin, malic acid, citric acid, vitamin C, artificial blackcurrant flavouring and low-nitrate water)
Treatment:
Other: Beverage: Placebo (sucrose, glucose, fructose, maltodextrin, malic acid, citric acid, vitamin C, artificial blackcurrant flavouring and low-nitrate water)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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