- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07674602
Effects of Fried Foods Prepared in Palm Oil Blended With Canola Oil Containing Surfactants and Green Tea Extract
June 23, 2026 updated by: Pornanong Aramwit, Pharm.D., Ph.D, Chulalongkorn University
Effects of Fried Foods Prepared in Palm Oil Blended With Canola Oil Containing Surfactants and Green Tea Extract on Postprandial Triglyceride Levels: A Double-blinded Randomized Controlled Clinical Trial
The objectives of the study were to investigate effects of foods prepared in palm oil blended with canola oil containing surfactants and green tea extract on postprandial triglyceride levels in healthy volunteers.
There were 22 subjects in the study.
They were divided into 2 groups: 1.comsumed foods fried in palm oil blended with canola oil containing surfactants and green tea extract and 2.comsumed foods fried in palm oil.
Postprandial triglyceride, lipid profiles, and liver and kidney functions were evaluated before and after taking 5 hours.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
22
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Bangkok, Thailand, 10330
- Chulalongkorn University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Male or female participants aged 18-60 years.
- Participants with fasting triglyceride levels <150 mg/dL (after fasting for at least 8-12 hours before blood collection).
- Participants without a history of cardiovascular disease, diabetes mellitus, thyroid disease, cancer, liver disease, or kidney disease.
- Participants who are able to read and write.
- Participants who voluntarily agree to participate after receiving information regarding the study objectives, procedures, potential risks, and expected benefits; are able to comply with the study protocol; and provide written informed consent.
Exclusion Criteria:
- Participants with a history of allergy or adverse reactions, such as skin, respiratory, or gastrointestinal symptoms, after consuming foods containing canola oil, polyglycerol esters of fatty acids (PGEs), green tea extract, palm oil, or banana.
- Participants who have consumed medications, dietary supplements, herbal products, or foods that may affect metabolism, such as weight-loss products or L-carnitine, within 2 weeks prior to enrollment.
- Participants who regularly use medications that may affect lipid metabolism or blood lipid levels, such as corticosteroids or lipid-lowering agents.
- Participants with serious underlying diseases or poorly controlled medical conditions, such as cancer, cardiovascular disease, or immunodeficiency disorders.
- Participants with impaired liver or kidney function, defined as AST/ALT levels >3 times the upper limit of normal or kidney disease with an estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m².
- Female participants who are pregnant or breastfeeding.
- Participants who regularly smoke.
- Participants who regularly consume alcohol.
- Participants who are currently participating in another research study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Fried Foods Prepared in Palm Oil Blended With Canola Oil Containing Surfactants and Green Tea Extrac
Take fried foods prepared in palm oil blended with canola oil containing surfactants and green tea extract 7 pieces.
|
Take fried foods prepared in palm oil blended with canola oil containing surfactants and green tea extract 7 pieces.
|
|
Active Comparator: Control group
Take fried foods prepared in palm oil 7 pieces
|
Take fried foods prepared in palm oil 7 pieces.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postprandial triglyceride
Time Frame: 5 hours
|
Postprandial triglyceride in blood
|
5 hours
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Total cholesterol in blood
Time Frame: 5 hours
|
5 hours
|
|
High Density Lipoprotein in blood
Time Frame: 5 hours
|
5 hours
|
|
Low Density Lipoprotein in blood
Time Frame: 5 hours
|
5 hours
|
|
Fasting blood glucose
Time Frame: 5 hours
|
5 hours
|
|
Creatinine in blood
Time Frame: 5 hours
|
5 hours
|
|
Blood Urea Nitrogen
Time Frame: 5 hours
|
5 hours
|
|
Aspartate Aminotransferase in blood
Time Frame: 5 hours
|
5 hours
|
|
Alanine Aminotransferase in blood
Time Frame: 5 hours
|
5 hours
|
|
Alkaline Phosphatase in blood
Time Frame: 5 hours
|
5 hours
|
|
Plasma antioxidant
Time Frame: 5 hours
|
5 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2025
Primary Completion (Actual)
March 31, 2026
Study Completion (Actual)
April 15, 2026
Study Registration Dates
First Submitted
June 23, 2026
First Submitted That Met QC Criteria
June 23, 2026
First Posted (Actual)
June 29, 2026
Study Record Updates
Last Update Posted (Actual)
June 29, 2026
Last Update Submitted That Met QC Criteria
June 23, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- EC25137-20
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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