- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05944029
Effect of Pomegranate Seed Powder on Markers of Metabolic Syndrome
Therapeutic Effects of Pomegranate Seed Powder on Metabolic Syndrome Markers
Study Overview
Status
Conditions
Intervention / Treatment
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.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Shahbano Zahid, Mphil
- Phone Number: +923095563643
- Email: shahbanozahid265@gmail.com
Study Contact Backup
- Name: Dr. Asif Ali, PhD
- Phone Number: 296 +923017151530
- Email: asif.ali@uvas.edu.pk
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54000
- Recruiting
- University of Veterinary and Animal sciences Lahore
-
Contact:
- Dr. Asif Ali, PhD
- Phone Number: 296 03017151530
- Email: asif.ali@uvas.edu.pk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Metabolic syndrome Patients
Pomegranate seed powder is administered for alleviating symptoms of metabolic syndrome
|
10 g powder / day
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lipid Profile
Time Frame: 7 weeks
|
The change in Lipid Profile, after consuming Pomegranate seed powder for 7 weeks will be assessed, to look for improvements.
|
7 weeks
|
|
Fasting Glucose
Time Frame: 7 weeks
|
The change in Blood Glucose level, after consuming Pomegranate seed powder for 7 weeks will be assessed, to look for improvements.
|
7 weeks
|
|
Blood Pressure
Time Frame: 7 weeks
|
The change in both systolic and diastolic blood pressure after consuming Pomegranate seed powder for 7 weeks will be assessed, to look for improvements.
|
7 weeks
|
|
Weight
Time Frame: 7 weeks
|
The change in weight, after consuming Pomegranate seed powder for 7 weeks will be assessed, to look for improvements.
|
7 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Dr. Asif Ali, Mphil, University of Veterinary and Animal sciences Lahore
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- UVAS (Other Identifier: UNIVERSITY OF VETERINARY & ANIMAL SCIENCES, LAHORE)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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