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The effect of sesame-canola oil compared to sesame and canola oil on patients with type 2 diabetes and their spouse

The effect of sesame-canola oil compared to sesame and canola oil on blood pressure, lipid profile and blood glucose control in patients with type 2 diabetes and their spouse: A three-way randomized cross-over clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016091312571N6
Enrollment
100
Registered
2016-11-14
Start date
2016-05-07
Completion date
Unknown
Last updated
2018-06-18

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

Conditions

Condition 1: Non-insulin-dependent diabetes mellitus. Condition 2: Spouses. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: Intervention: Sesame-canola oli. Intervention 2: control: sesame oil. Intervention 3: Control: Canola oil.

Sponsors

Vice Chancellor for Research, shahid sadughi yazd University of Medical Sciences
Lead Sponsor
Neshatavar food industry (Datis)
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Adults aged between 18-60 years old With clinically diagnosed type 2 diabetes for at least 6-month and maximum of 10 years With hemoglubin A1C lower than 8 percent Only take oral anti-hyperglycemic agents for the treatment have intention to enter the study and fill the informed consent

Exclusion criteria

Exclusion criteria: Being on insulin therapy History of known Cardiovascular Diseases (Coronary Artery Disease, Stroke, Congestive heart disease) Coronary artery bypass grafting (CABG) History of kidney or liver disease [alanine aminotransferase (ALT) and aspartate aminotransferase (AST) three times more than normal values] history of cancer Changing the dose of lipid lowering medications for at least 3 months prior starting the study being pregnant

Design outcomes

Primary

MeasureTime frame
Serum high density lipoprotein cholesterol (HDL-C). Timepoint: start and the end of each intervention period. Method of measurement: Using Appropriate kits, by Alpha-Classic autoanalyzer.;Serum fasting blood sugar(FBS). Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate kits, by Alpha-Classic autoanalyzer.;Serum low Density Lipoprotein cholesterol (LDL-C). Timepoint: start and the end of each intervention period. Method of measurement: Using Appropriate kits, by Alpha-Classic autoanalyzer.;Serum Total cholesterol. Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate kits, by Alpha-Classic autoanalyzer.;Serum triglyceride level (TG). Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate kits, by Alpha-Classic autoanalyzer.

Secondary

MeasureTime frame
BMI(body mass index). Timepoint: entrance and start and the end of each intervention period. Method of measurement: kg/m2.;Body Fat percent. Timepoint: entrance and start and the end of each intervention period. Method of measurement: by body composition analyzer.;Muscle mass percent. Timepoint: entrance and start and the end of each intervention period. Method of measurement: by body composition analyzer.;Weight. Timepoint: entrance and start and the end of each intervention period. Method of measurement: by body Calibrated scale.;Blood pressure. Timepoint: entrance and start and the end of each intervention period. Method of measurement: by Barometer.;Insulin. Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate ELISA kit.;Lipoprotein(a). Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate kits, by Alpha-Classic autoanalyzer.;Apo lipoprotein A (Apo A). Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate kits, by Alpha-Classic autoanalyzer.;Apo lipoprotein B(Apo B). Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate kits, by Alpha-Classic autoanalyzer.;Alkaline phosphatase ( ALP). Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate kits, by Alpha-Classic autoanalyzer.;Alanine aminotransferase (ALT). Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate kits, by Alpha-Classic autoanalyzer.;Aspartate aminotransferase (AST). Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate kits, by Alpha-Classic autoanalyzer.;Gama glutamil transferase (GGT). Timepoint: start and the end of each intervention period. Method of measurement: using Appropriate kits, by Alpha-Classic autoanalyzer.;Urea. Timepoint: start and the end of each intervention peri

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMojgan Amiri

Nutrition and Food security Research Center, Faculty of Health, Shahid Sadoughi University of Medica

mojgan.amiri2015@yahoo.com+98 35 3820 9100

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 18, 2026