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

NCT ID: NCT00728299

Last Updated: 2008-08-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 384 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-09-30
• Study Completion Date: 2005-09-30

Brief 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.

Detailed 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]).

Conditions

Coronary Artery Disease

Keywords

Coronary artery disease, carotid intima-media thickness

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: QUADRUPLE

Study Groups

1

Group Type: EXPERIMENTAL

PomWonderful Juice

Intervention Type: DRUG

8 oz per day each day for 78 weeks

2

Group Type: PLACEBO_COMPARATOR

Placebo juice

Intervention Type: DRUG

8 oz per day for 78 weeks

Interventions

PomWonderful Juice

8 oz per day each day for 78 weeks

Intervention Type: DRUG

Placebo juice

8 oz per day for 78 weeks

Intervention Type: DRUG

Eligibility Criteria

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).

• Minimum Eligible Age: 45 Years
• Maximum Eligible Age: 74 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Roll International Corporation

INDUSTRY

Sponsor Role: collaborator

Radiant Research

OTHER

Sponsor Role: lead

Responsible Party

Radiant Research

Principal Investigators

Michael H Davidson, MD

Role: PRINCIPAL_INVESTIGATOR

FACC

Other Identifiers

Radiant Development #202528

Identifier Type: -

Identifier Source: org_study_id