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Effect of Cranberry Juice on Endothelial Function

Long-Term Effects of Cranberry Juice on Endothelial Function in Patients With Coronary Artery Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00553904
Enrollment
40
Registered
2007-11-06
Start date
2008-02-29
Completion date
2009-05-31
Last updated
2009-06-18

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

Conditions

Coronary Artery Disease

Brief summary

A pilot study of 15 subjects will be completed to determine whether acute consumption of cranberry juice has an effect on endothelial function. We will then complete a randomized, double blind, placebo controlled crossover study designed to investigate the effects of cranberry juice consumption on endothelial function. Participants (n=40) will drink 480 ml of double strength cranberry juice or a similar appearing and tasting placebo per day for four weeks. After a two week rest period, they will cross over to the other beverage. We will examine endothelial function before and after each of the two treatment periods. The study will provide information about the chronic vascular effects of cranberry juice.

Interventions

DIETARY_SUPPLEMENTCranberry juice

480 ml of double strength cranberry juice daily for four weeks

Sponsors

Boston University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Coronary artery disease

Exclusion criteria

* Pregnant and lactating women * Clinical history of other major illness including end-stage cancer, renal failure, hepatic failure, gastrointestinal disorders that may impair absorption, or other conditions that in the opinion of the principal investigator make a clinical study inappropriate * Treatment with an investigational new drug within the last 30 days * History of a psychological illness or condition such as to interfere with the subject's ability to understand the requirements of the study. * Treatment with Vitamin E, Vitamin C, beta carotene, lipoic acid, or other food or herbal supplements within 2 weeks of enrollment (subjects taking multivitamins or other forms of vitamin E and C in doses that do not exceed two times the RDA will not be excluded).

Design outcomes

Primary

MeasureTime frame
Brachial artery flow-mediated dilation1 month

Secondary

MeasureTime frame
Carotid-femoral pulse wave velocity1 month
Markers of inflammation1 month
Serum anthocyanins1 month

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026