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Pomegranate Juice and Metabolic Syndrome

The Effect of Pomegranate Juice Intake on Cardiometabolic Factors in Subjects With Metabolic Syndrome.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02298621
Enrollment
30
Registered
2014-11-24
Start date
2013-01-31
Completion date
2013-02-28
Last updated
2014-11-24

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

Conditions

Metabolic Syndrome

Brief summary

The effect of pomegranate juice (PJ) intake on cardiovascular risks in subject with metabolic syndrome.

Detailed description

The effect of pomegranate juice (PJ) intake on cardiovascular risks in subject with metabolic syndrome in shabestar.

Interventions

OTHERpomegranate juice

Randomized clinical trial or RCT

OTHERplacebo

Randomized clinical trial or RCT

Sponsors

Urmia University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* presence of ≥3 of the following diagnostic of MetS: * serum TGs of at least 150 mg/dL, * waist circumference of more than 102 cm (40 in) in men and more than 88 cm (35 in) in women, * high-density lipoprotein (HDL) level less than 40 mg/dL in men and less than 50 mg/dL in women, * blood pressure 135/85 mm Hg or higher, or * fasting glucose 100 mg/dL or Higher

Exclusion criteria

* liver cirrhosis, * chronic pancreatitis, * gastrointestinal or connective diseases, * kidney stones, or * renal failure, * alcohol Consumption, * having an allergy to pomegranate juice, * a change in diet, * the large increase in LDL so that required drug treatment. * use of statins of fibrates, corticosteroids, nitrates, acetyl-salicylic acid or other anti-platelet drugs, oral hypoglycemic drugs, nonsteroidal anti-inflammatory drugs, or drugs interfering with coagulation; * pregnancy or lactation in the past 6 mo, supplementation with vitamins or antioxidants

Design outcomes

Primary

MeasureTime frame
Change from baseline in values of metabolic syndrome components at 1 week1 week

Secondary

MeasureTime frameDescription
Change from baseline in values of insulin resistance (HOMA-IR), total cholesterol, LDL-C, VLDL-C and hs-CRP at 1 week1 weeksInsulin resistance via HOMA-IR

Countries

Iran

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026