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Effects of Fried Foods Prepared in Palm Oil Blended With Canola Oil Containing Surfactants and Green Tea Extract

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07674602
Enrollment
22
Registered
2026-06-29
Start date
2025-11-01
Completion date
2026-04-15
Last updated
2026-06-29

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

Conditions

Healthy Adult Participants

Keywords

Healthy, canola, surfactant, green tea

Brief summary

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.

Interventions

OTHERFried Foods Prepared in Palm Oil Blended With Canola Oil Containing Surfactants and Green Tea Extract

Take fried foods prepared in palm oil blended with canola oil containing surfactants and green tea extract 7 pieces.

OTHERFried Foods Prepared in Palm Oil

Take fried foods prepared in palm oil 7 pieces.

Sponsors

Chulalongkorn University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Postprandial triglyceride5 hoursPostprandial triglyceride in blood

Secondary

MeasureTime frame
Total cholesterol in blood5 hours
High Density Lipoprotein in blood5 hours
Low Density Lipoprotein in blood5 hours
Fasting blood glucose5 hours
Creatinine in blood5 hours
Blood Urea Nitrogen5 hours
Aspartate Aminotransferase in blood5 hours
Alanine Aminotransferase in blood5 hours
Alkaline Phosphatase in blood5 hours
Plasma antioxidant5 hours

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 30, 2026