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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02192047
Other study ID # PD 174/13
Secondary ID
Status Completed
Phase N/A
First received June 24, 2014
Last updated July 15, 2014
Start date September 2012
Est. completion date March 2014

Study information

Verified date July 2014
Source Malaysia Palm Oil Board
Contact n/a
Is FDA regulated No
Health authority Malaysia: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The investigators hypothesized that there will be a significant difference between the effects of trans-free palm-, interesterified palm- and interesterified soybean oil blend on cardiovascular disease, inflammation, insulin resistance and obesity.


Description:

Human volunteers will be conditioned for a 8 wk intervention on 3 different test diets providing 30 % energy as fat, 15% energy as protein and 55% energy as carbohydrate according to parallel designed sequences. The test fats used for this study are palm oil, chemically interesterified palm oil and chemically interesterified fully hydrogenated soybean oil and soft oil blend in the form of margarine. Volunteers will be restricted to follow the dietary guidelines throughout the study. Blood collection sessions will held before and after every diet intervention. Outcome measures of the study are serum lipid profile, markers of inflammation, markers of obesity and insulin resistance.


Recruitment information / eligibility

Status Completed
Enrollment 85
Est. completion date March 2014
Est. primary completion date March 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- Adult males and females, aged 20-60 yr

- Staff and students of International Medical University, IMU/ Staff of Malaysian Palm Oil Board, MPOB to facilitate centralized consumption of the test fats/snacks

- BMI 21 - 30 kg/m2

Exclusion Criteria:

- Abnomal liver function test (elevated transaminases- alanine aminotransferase,ALT; aspartate aminotransferase,AST))/ abnormal kidney function test (elevated plasma creatinine)

- History of type 2 diabetes mellitus, cancer, stomach ulcers, drug abuse or alcoholism

- Smokers

- On lipid/blood pressure- lowering medication/supplements

- Blood pressure>140/90 mmHg

- Fasting total cholesterol > 6.5 mmol/L

- Fasting TAG > 2.0 mmol/L

- Candidates who are going abroad during the planned schedule for the dietary intervention

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
Palm Olein
8 weeks
IE Palm olein
8 weeks
IE soybean oil-based
8 weeks

Locations

Country Name City State
Malaysia University Putra Malaysia Serdang Selangor

Sponsors (3)

Lead Sponsor Collaborator
Malaysia Palm Oil Board International Medical University, Universiti Putra Malaysia

Country where clinical trial is conducted

Malaysia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in serum C-peptide level of subject up to 8 weeks No
Secondary Change in serum lipid profile up to 8 weeks No
Secondary Change in markers of inflammation up to 8 weeks No
Secondary Change in markers of obesity up to 8 weeks No
Secondary Change in markers of insulin resistance up to 8 weeks No
Secondary Oral Glucose tolerance test (OGTT) Baseline, month-2 No
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