The Effects of Consumption of Pomegranate Juice on Carotid Intima-Media Thickness

Coronary Artery Disease Clinical Trial

Official title:

The Effects of Consumption of Pomegranate Juice on Carotid Intima-Media Thickness

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00728299
• Other study ID #: Radiant Development #202528
• Status: Completed
• Phase: N/A
• First received: July 31, 2008
• Last updated: August 4, 2008
• Start date: September 2003
• Est. completion date: September 2005

Study information

• Verified date: August 2008
• Source: Radiant Research
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

Increases in carotid artery intima-media thickness (IMT) are correlated with increased risk of stroke and myocardial infarction. The purpose of this study is to assess if pomegranate juice will retard the carotid (IMT) progression rate in men and women who have one or more existing cardiovascular risk factors (current cigarette smoking, hypertension, low HDL-cholesterol, and/or high LDL-cholesterol) upon entrance into the study.

Description:

Previous studies in atherosclerotic mice have shown that pomegranate supplementation reduced their macrophage oxidative stress and attenuated the development of their atherosclerosis. Further research in hypertensive humans demonstrated that pomegranate juice had an angiotensin converting enzyme (ACE)-inhibitory effect and significantly decreased systolic blood pressure.

This study will use a randomized, double-blind, placebo-controlled design with eight clinic visits (one screening visit [week -4 to -1], one baseline visit [week 0], and six treatment visits [weeks 13, 26, 38, 52, 65, and 78]).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 384
• Est. completion date: September 2005
• Est. primary completion date: September 2005
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 45 Years to 74 Years

Eligibility

Inclusion Criteria:

• Males between the ages of 45 and 74 and females between the ages of 55 and 74 years.

• Subject has = 1 of the following risk factors at Visit 1 (week -4 to -1):

• current cigarette smoking (defined as any cigarette smoking within the past month)

• hypertension (blood pressure = 140/90 mm Hg or using an antihypertensive medication)

• low HDL cholesterol (< 40 mg/dL)

• high LDL cholesterol (= 130 mg/dL and < 190 mg/dL), on statin therapy or not

• Posterior wall common carotid IMT > 0.7 mm and < 2.0 mm at Visit 2 (week 0) with an adequate image on at least one side.

• Subject understands the study procedures and signs an informed consent form.

• Normally active and judged to be in good health on the basis of medical history, physical examination, and routine laboratory tests.

Exclusion Criteria:

• Use of any pharmacologic lipid-altering medications, besides statins (e.g., fibrate derivatives, bile acid binding resins, and niacin or its analogues at doses > 400 mg/d) six weeks prior to Visit 1

• Body mass index > 40 kg/m2.

• Unstable use (< 2 months prior to Visit 1) of any supplement known to alter lipid metabolism, including but not limited to: dietary fiber supplements (including > 2 teaspoons Metamucil® or psyllium-containing supplement per day), omega-3 fatty acid supplements, sterol/stanol products, red rice yeast supplements, garlic supplements, soy isoflavone supplements or others at the discretion of the Investigator).

• History of pomegranate consumption (either eating pomegranates or drinking pomegranate juice) within the past 6 months.

• Clinical evidence or history of coronary heart disease (CHD) or CHD equivalents including:

• diabetes mellitus,

• angina,

• myocardial infarction,

• transient ischemic attack,

• symptomatic carotid artery disease,

• cerebrovascular accident,

• coronary artery bypass grafting,

• percutaneous transluminal coronary angioplasty,

• peripheral arterial disease,

• abdominal aortic aneurysm,

• ankle brachial index < 0.90,

• and/or a Framingham Risk Score = 16 points for men and = 23 points for women (10-year CHD risk > 20%)

• Active cancer, other than non-melanoma skin cancer, within the previous two years.

• Prior diagnosis of human immunodeficiency virus (HIV) or hepatitis B or hepatitis C.

• Uncontrolled hypertension (average systolic blood pressure = 160 mm Hg and/or average diastolic blood pressure = 100 mm Hg).

• Untreated or unstable hypothyroidism (receiving stable dose therapy for < 4.0 months).

• Concomitant use of beta-adrenergic blockers or immunosuppressants

• Concomitant use of estrogen or progestin therapy.

• Allergy to pomegranates or pomegranate juice.

• Known allergy to blood products.

• Non-English speaking.

• Active liver disease or hepatic dysfunction as defined by elevations of = 2.0 x ULN at Visit 1 in any of the following liver function tests: ALT, AST or bilirubin.

• Serum creatinine > 2.0 mg/dL recorded during screening period.

• Recent history of (within past 12 months) or strong potential for alcohol or substance abuse. Alcohol abuse will be defined as >14 drinks per week (1 drink = 12 oz beer, 4 oz wine, or 1 ½ oz distilled spirits).

• Participation in another clinical study within 30 days prior to screening visit 1 (week -4 to -1).

• Has a condition the Investigator believes would interfere with evaluation of the subject, or may put subject at undue risk.

• Posterior wall common carotid IMT = 2.0 mm on either side at Visit 2 (week 0).

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Coronary Artery Disease
• Coronary Disease
• Myocardial Ischemia

Intervention

Drug:
• PomWonderful Juice
8 oz per day each day for 78 weeks
• Placebo juice
8 oz per day for 78 weeks

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
Radiant Research	Roll International Corporation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Difference in posterior wall common carotid intima-media thickness (IMT) progression rate in mm/yr between PomWonderful juice and placebo, utilizing non-contrast images		78-90 weeks	No
Secondary	Difference between placebo and PomWonderful juice in internal carotid artery IMT progression rate in mm/yr		78-90 weeks	No
Secondary	Difference between placebo and PomWonderful juice in the carotid bifurcation IMT progression rate in mm/yr		78-90 weeks	No
Secondary	Difference between placebo and PomWonderful juice in the anterior wall common carotid IMT progression rate in mm/yr, without contrast agent		78-90 weeks	No
Secondary	Difference between placebo and PomWonderful juice in the anterior wall common carotid IMT progression rate in mm/yr, with contrast agent		78-90 weeks	No
Secondary	Difference between placebo and PomWonderful juice in the posterior wall common carotid IMT progression rate in mm/yr, with contrast agent		78-90 weeks	No
Secondary	Difference between placebo and PomWonderful juice in the composite IMT measure, which combines the measurements of the common and internal carotid and the carotid bifurcation in mm/yr		78-90 weeks	No
Secondary	Change from baseline to 13 weeks in hs-CRP concentration		13 weeks	No