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Pomegranate Supplementation on Physical Function and Cardiovascular Disease Risk in CKD Patients

Primary Purpose

Chronic Kidney Disease, Cardiovascular Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pomegranate extracts
Sponsored by
Kenneth Wilund
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Chronic Kidney Disease

Eligibility Criteria

30 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1) Subjects must be diagnosed with CKD stage 3, 4 or 5 (glomerular filter rate < 59 mL/min).
  • 2) Subjects must be ≥ 30 years of age, to increase the probability of having developed significant arterial stiffness.
  • 3) Subjects must be willing to be randomized to the control or intervention groups. The health history questionnaire and PAR-Q will be used to determined eligibility.

Subjects must complete a medical history and a nephrologist must sign off on a medical clearance for the subject before they can begin the study.

Exclusion Criteria:

  • 1) Subjects < 30 years of age.
  • 2) Subjects who are not willing to be randomized to one of the two groups.

Sites / Locations

  • Champaign-Urbana Dialysis Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Pre-diaylsis patients

Dialysis patients

Arm Description

Chronic Kidney Disease patients not receiving dialysis getting pomegrante Supplementation

Chronic Kidney Disease patients receiving dialysis getting pomegranate supplementation

Outcomes

Primary Outcome Measures

Markers of oxidative stress
Markers of inflammation

Secondary Outcome Measures

Cardiovascular risk
Muscular performance

Full Information

First Posted
March 9, 2011
Last Updated
December 13, 2013
Sponsor
Kenneth Wilund
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1. Study Identification

Unique Protocol Identification Number
NCT01324193
Brief Title
Pomegranate Supplementation on Physical Function and Cardiovascular Disease Risk in CKD Patients
Official Title
Effects of Pomegranate Supplementation on Physical Function and Cardiovascular Disease Risk in Chronic Kidney Disease Patients
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Kenneth Wilund

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Chronic kidney disease (CKD) patients have very low physical function and high rates of cardiovascular disease (CVD) mortality. The objective of the proposed research is to evaluate the effects of dietary supplementation with a pomegranate extract, that contains high amounts of antioxidants, on physical function and CVD risk. Patients with moderate to severe chronic kidney disease that are NOT yet on dialysis tend to have significantly reduced risk factors for cardiovascular disease (and other disorders) compared to dialysis patients. This includes significantly reduced systemic markers of oxidative stress and inflammation. As a result, therapies designed to reduce the risk of CKD co-morbidities may differ significantly in dialysis and pre-dialysis patients. For example, dialysis patients are recommended to INCREASE their intake of dietary protein, while pre-dialysis patients are recommended to DECREASE their protein intake, due to differences in the pathophysiology of the two conditions. The investigators have decided to recruit pre-dialysis patients in addition to dialysis patients in this study because the investigators believe this will help us determine if the efficacy of pomegranate differs between patients with different stages of CKD.
Detailed Description
Chronic kidney disease (CKD) patients have very low physical function and high rates of cardiovascular disease (CVD) mortality. The objective of the proposed research is to evaluate the effects of dietary supplementation with a pomegranate extract, that contains high amounts of antioxidants, on physical function and CVD risk. Patients with moderate to severe chronic kidney disease that are NOT yet on dialysis tend to have significantly reduced risk factors for cardiovascular disease (and other disorders) compared to dialysis patients. This includes significantly reduced systemic markers of oxidative stress and inflammation. As a result, therapies designed to reduce the risk of CKD co-morbidities may differ significantly in dialysis and pre-dialysis patients. For example, dialysis patients are recommended to INCREASE their intake of dietary protein, while pre-dialysis patients are recommended to DECREASE their protein intake, due to differences in the pathophysiology of the two conditions. The investigators have decided to recruit pre-dialysis patients in addition to dialysis patients in this study because the investigators believe this will help us determine if the efficacy of pomegranate differs between patients with different stages of CKD. CKD patients will be recruited under 2 phases: CKD patients not receiving dialysis treatment (pre-dialysis patients) will be recruited in the first phase. This will include patients with CKD stage 3-5 that are not yet on dialysis. In the second phase, only CKD patients on dialysis treatment will be recruited. To address these questions, CKD patients will be randomized to the following groups for 12 months: 1) no POM supplementation/control (CON), and 2) oral supplementation with purified pomegranate extract (POM). Patients in the POM group will ingest a 1000 milligram capsule of POM extract, 7 days per week. Patients in the CON group will receive a placebo capsule using the same protocol. On three occasions, at baseline, 6, and 12 months, each subject will have blood collected to measure plasma markers of oxidative stress (TBARS, lipid peroxides), blood lipid levels, and glucose and insulin levels. Arterial and cardiac structure and function will be measured by vascular ultrasound and echocardiogram, respectively. A 24-hour dietary recall will be used to assess the intake of nutrients. Leg strength will be measured on a resistance exercise machine. Bone density and body composition will be evaluated using dual energy x-ray absorptiometry (DXA). Pre-dialysis subjects will undergo a maximal exercise test to assess their cardiorespiratory fitness level. In dialysis patients, instead of a maximal exercise test, physical function will be measured by a 6-item functional fitness assessment and a 10-meter walk test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease, Cardiovascular Disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
33 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pre-diaylsis patients
Arm Type
Other
Arm Description
Chronic Kidney Disease patients not receiving dialysis getting pomegrante Supplementation
Arm Title
Dialysis patients
Arm Type
Other
Arm Description
Chronic Kidney Disease patients receiving dialysis getting pomegranate supplementation
Intervention Type
Dietary Supplement
Intervention Name(s)
Pomegranate extracts
Intervention Description
a 1000mg capsule of a purified pomegranate polyphenol supplement (POMx™, POM Wonderful, Inc. Los Angeles, CA)7 days a week for 12 months.
Primary Outcome Measure Information:
Title
Markers of oxidative stress
Time Frame
Circulating markers of oxidative stress will be reduced and serum antioxidant activity will be increased in POM, compared to CON after 12 months of intervention.
Title
Markers of inflammation
Time Frame
Circulating markers of inflammation will be reduced in POM, compared to CON after 12 months of intervention.
Secondary Outcome Measure Information:
Title
Cardiovascular risk
Time Frame
Carotid artery stiffness and CIMT will be reduced in POM compared to CON after 12 months.
Title
Muscular performance
Time Frame
Muscle strength and physical performance will be reduced in CON compared to POM after 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1) Subjects must be diagnosed with CKD stage 3, 4 or 5 (glomerular filter rate < 59 mL/min). 2) Subjects must be ≥ 30 years of age, to increase the probability of having developed significant arterial stiffness. 3) Subjects must be willing to be randomized to the control or intervention groups. The health history questionnaire and PAR-Q will be used to determined eligibility. Subjects must complete a medical history and a nephrologist must sign off on a medical clearance for the subject before they can begin the study. Exclusion Criteria: 1) Subjects < 30 years of age. 2) Subjects who are not willing to be randomized to one of the two groups.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kenneth Wilund, PhD
Organizational Affiliation
University of Illinois at Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
Champaign-Urbana Dialysis Center
City
Champaign
State/Province
Illinois
ZIP/Postal Code
61820
Country
United States

12. IPD Sharing Statement

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Pomegranate Supplementation on Physical Function and Cardiovascular Disease Risk in CKD Patients

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