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Effect of Pomegranate Seed Powder on Markers of Metabolic Syndrome

Therapeutic Effects of Pomegranate Seed Powder on Metabolic Syndrome Markers

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05944029
Enrollment
50
Registered
2023-07-13
Start date
2023-02-20
Completion date
2023-08-24
Last updated
2023-07-13

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

Conditions

Metabolic Syndrome

Keywords

Metabolic Syndrome, Hypertension, Obesity, Insulin Resistance, Diabetes, Pomegranate seed powder, Dyslipidemia

Brief summary

Metabolic syndrome is a public health concern worldwide and in Pakistan as well. Abdominal obesity, hyperglycemia, hypertriglyceridemia, hypertension, and low HDL cholesterol are its hallmarks while pomegranate seed's unique chemical composition has sparked research into the health benefits in same arena as weight control, blood lipid profile changes, and other metabolic disturbances. It's high time to study therapeutic efficiency of Pomegranate seed powder against metabolic syndrome.

Detailed description

Metabolic syndrome, accumulation of certain metabolic risk factors, such as abdominal obesity, hyperglycemia, hypertriglyceridemia, hypertension, and low HDL cholesterol, has been noted as one of the most important risk factors for the epidemic of type 2 diabetes and cardiovascular disease in the 21st century. It has become a significant public health concern and a global epidemic with a prevalence rate of about 25% among American adults. Multiple researches have demonstrated the effectiveness of pomegranate in the management of diabetes, inflammatory conditions, obesity, and blood lipid levels, and consequently metabolic syndrome. Various pomegranate components have the potential to substitute anti-diabetic medications as well Pomegranate seed's unique chemical composition has sparked research into the health benefits, such as weight control, blood lipid profile changes, and other metabolic disorders. seed powder can influence the patient's metabolic syndrome-related indicators. Hypothesis: Pomegranate seed powder can be effective to treat the individuals with impaired metabolism. Methodology: In a clinical trial, patients of metabolic syndrome (n=50) will be given pomegranate seed powder dose for over 8 weeks, twice a day. Biochemical outcomes including blood pressure, FBG, cholesterol, hemoglobin level will be determined before and after the completion of trial in addition to patient's weight. Finally, using one-way ANOVA and T-test, collected data will be analyzed. Expected outcome: The study will explore the potential of pomegranate seed powder in treating metabolic syndrome's risk factors. Therefore, our findings on the studied parameters of patient will assist future researchers in developing tested, evidence-based recommendations.

Interventions

DIETARY_SUPPLEMENTPomegranate seed powder

10 g powder / day

Sponsors

Asif Ali
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Prospective Clinical Trial

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* BMI \> 25kg/m2 * Dyslipidemia * Altered blood glucose level * Age 30-55 ( male and female)

Exclusion criteria

* Thyroid disorder * Liver disease * Kidney disorder * Cancer etc

Design outcomes

Primary

MeasureTime frameDescription
Lipid Profile7 weeksThe change in Lipid Profile, after consuming Pomegranate seed powder for 7 weeks will be assessed, to look for improvements.
Fasting Glucose7 weeksThe change in Blood Glucose level, after consuming Pomegranate seed powder for 7 weeks will be assessed, to look for improvements.
Blood Pressure7 weeksThe change in both systolic and diastolic blood pressure after consuming Pomegranate seed powder for 7 weeks will be assessed, to look for improvements.
Weight7 weeksThe change in weight, after consuming Pomegranate seed powder for 7 weeks will be assessed, to look for improvements.

Countries

Pakistan

Contacts

Primary ContactShahbano Zahid, Mphil
shahbanozahid265@gmail.com+923095563643
Backup ContactDr. Asif Ali, PhD
asif.ali@uvas.edu.pk+923017151530

Outcome results

None listed

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