Inflammation Clinical Trial
— POM PilotOfficial title:
A Pilot Trial Assessing the Effect of Pomegranate Juice and Extract on Biomarkers of Oxidative Stress, Systemic Inflammation, and Monocyte Function in Hemodialysis Patients
Verified date | May 2015 |
Source | University of Washington |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
In this study, the investigators will administer pomegranate juice or fruit extract as a
targeted antioxidant therapy to hemodialysis patients.
The investigators will examine whether these pomegranate products will be safe and
well-tolerated. The investigators will also examine whether these products may lead to
improvements in blood serum biomarkers of:
- oxidative stress status
- inflammatory status
- endothelial dysfunction
Status | Completed |
Enrollment | 24 |
Est. completion date | December 2012 |
Est. primary completion date | December 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 85 Years |
Eligibility |
Inclusion Criteria: - Patients with end-stage renal disease receiving thrice weekly hemodialysis - Age > 18 or < 85 years - Life expectancy greater than one year - Ability to understand and provide informed consent for participation in the study Exclusion Criteria: - History of poor adherence to hemodialysis or medical regimen - Prisoners, patients with significant mental illness, and other vulnerable populations - AIDS (HIV seropositivity is not an exclusion criteria) - Active malignancy excluding basal cell carcinoma of the skin - Gastrointestinal dysfunction requiring parenteral nutrition - History of functional kidney transplant < 6 months prior to study entry - Anticipated live donor kidney transplant - Patients taking vitamin E supplements > 60 IU/day, vitamin C > 150 mg/day or other antioxidant or nutritional supplements - Incident hemodialysis patients (defined as within 30 days of dialysis initiation) - Patients hospitalized for more than 5 days within the past 30 days. - Patients with a history of a major atherosclerotic event (defined as combined incidence of myocardial infarction, urgent target-vessel revascularization, coronary bypass surgery, and stroke) within three months - Pregnancy |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | Northwest Kidney Centers | Seattle | Washington |
Lead Sponsor | Collaborator |
---|---|
University of Washington |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Markers of oxidative stress | Oxidative stress: F2-isoprostanes | 12 weeks | No |
Primary | Markers of inflammation | Inflammation: C-reactive protein, Interleukin-6, and white blood cell count | 12 weeks | No |
Primary | Markers of endothelial function | Endothelial function: Monocyte functional assays (cytokines) | 12 weeks | No |
Secondary | Number of subjects with adverse events and type of event | Adverse reactions to pomegranate juice Adverse reactions to pomegranate fruit extract |
12 weeks | Yes |
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