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OpenTrials
Completed

NCT Number: NCT02984319

Effect of Cherry Concentrate on Vascular Function

Acute effect of cherry concentrate consumption on flow mediated dilatation in healthy young men

Completed

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Key information

Conditions

Healthy

Age range

18 year–30 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Sport & Health Sciences

Exeter, Devon, EX1 2LU, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • no prescription medications

Exclusion criteria

  • prescription medications

Treatment and study plan

Cherry versus placebo concentrate

Dietary Supplement

Acute cherry concentrate

Primary outcomes

  1. Flow mediated dilatation

    Time frame: Change from baseline to 3 hours post dietary supplementation

Secondary outcomes

  1. Microvascular function (laser doppler flowmetry)

    Time frame: Change from baseline to 3 hours post dietary supplementation

  2. Plasma nitrite concentration

    Time frame: Change from baseline to 3 hours post dietary supplementation

Sponsors and collaborators

Lead sponsor

University of Exeter

Other

Registry information

Important dates

Study start
2015
Primary completion
2018
Study completion
2018
First posted
Dec 6, 2016
Registry last updated
Oct 25, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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