Effects of Canola Oil on Blood Vessel Function in Peripheral Arterial Disease
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ClinicalTrials.gov Identifier: NCT01250275 |
Recruitment Status :
Completed
First Posted : November 30, 2010
Last Update Posted : March 27, 2013
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Condition or disease | Intervention/treatment | Phase |
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Peripheral Arterial Disease | Other: traditional canola oil Other: high oleic canola oil Other: soybean oil Other: high linoleic safflower oil Other: coconut oil Other: safflower oil | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 53 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Triple (Participant, Care Provider, Investigator) |
Official Title: | Effects of Canola Oil on Blood Vessel Function in Peripheral Arterial Disease (PAD) |
Study Start Date : | September 2011 |
Actual Primary Completion Date : | December 2012 |
Actual Study Completion Date : | February 2013 |

Arm | Intervention/treatment |
---|---|
Experimental: Acute Phase: traditional canola oil
Participants will receive banana bread containing traditional canola oil once weekly during the 5-week schedule
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Other: traditional canola oil
Participants (10 healthy and 10 with peripheral arterial disease) will be asked to attend a total of 5 consecutive visits (with a minimum of 6 days between visits) in a fasting state where they will be randomly assigned one food item in the form of banana bread containing 50 gm fat from traditional canola oil. |
Active Comparator: Acute Phase: high oleic canola oil
Participants will receive banana bread containing high oleic canola oil once weekly during the 5-week schedule
|
Other: high oleic canola oil
Participants (10 healthy and 10 with peripheral arterial disease) will be asked to attend a total of 5 consecutive visits (with a minimum of 6 days between visits) in a fasting state where they will be randomly assigned one food item in the form of banana bread containing 50 gm fat from high oleic canola oil. |
Active Comparator: Acute Phase: soybean oil
Participants will receive banana bread containing soybean oil once weekly during the 5-week schedule
|
Other: soybean oil
Participants (10 healthy and 10 with peripheral arterial disease) will be asked to attend a total of 5 consecutive visits (with a minimum of 6 days between visits) in a fasting state where they will be randomly assigned one food item in the form of banana bread containing 50 gm fat from soybean oil. |
Active Comparator: Acute Phase: high linoleic safflower oil
Participants will receive banana bread containing high linoleic safflower oil once weekly during the 5-week schedule
|
Other: high linoleic safflower oil
Participants (10 healthy and 10 with peripheral arterial disease) will be asked to attend a total of 5 consecutive visits (with a minimum of 6 days between visits) in a fasting state where they will be randomly assigned one food item in the form of banana bread containing 50 gm fat from high linoleic safflower oil. |
Active Comparator: Acute Phase: coconut oil
Participants will receive banana bread containing coconut oil once weekly during the 5-week schedule
|
Other: coconut oil
Participants (10 healthy and 10 with peripheral arterial disease) will be asked to attend a total of 5 consecutive visits (with a minimum of 6 days between visits) in a fasting state where they will be randomly assigned one food item in the form of banana bread containing 50 gm fat from coconut oil. |
Experimental: Chronic Phase: traditional canola oil
A total of 25 participants with peripheral arterial disease will be assigned foods containing traditional canola oil for a total of 8 weeks
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Other: traditional canola oil
Participants with peripheral arterial disease (n=25) will be randomized to daily consumption of food items prepared with traditional canola oil for eight weeks. |
Active Comparator: Chronic Phase: safflower oil
A total of 25 participants with peripheral arterial disease will be assigned foods containing an oil mixture representing the typical western diet for a total of 8 weeks
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Other: safflower oil
Participants with peripheral arterial disease (n=25) will be randomized to daily consumption of foods prepared with an oil mixture representing the typical western diet |
- Acute study to identify the relative potency of fatty acid compositions on blood vessel function in healthy participants and individuals with peripheral arterial disease. [ Time Frame: weekly testing for 5 weeks ]Participants (n=20,10 peripheral arterial disease/10 healthy) will attend 5 weekly visits and receive one food item (banana bread)at each visit. Assessment of endothelial function at 2-hours post consumption. Blood samples will be collected for plasma triglycerides, glucose, insulin, markers of oxidative stress, vascular function, inflammation, and metabolism. Food intake and physical activity will be recorded the day before their first test visit, and the same (foods and activities) will be repeated before each visit. Ankle Brachial Index and Pulse Wave Velocity testing will be done.
- To test the effects of canola oil consumption for its effects on vascular function and cardiovascular risk factors in a chronic 8-week study in individuals with peripheral arterial disease. [ Time Frame: baseline and at 8 weeks ]Participants (n=50,peripheral arterial disease) will be randomly assigned (25 per group) to food items containing either traditional canola oil or an oil mixutre representing the Western diet. Assessments of vascular function, cognitive function, blood lipid profile, glycated hemoglobin, biomarkers of vascular function, inflammation, oxidative stress, immune function, and metabolism, advanced glycated endproducts, and anthropometrics will be completed at baseline and at 8 weeks.
- To explore whether improvements in blood vessel function in the chronic 8-week study are also associated with improvements in cognitive function. [ Time Frame: baseline and at 8 weeks ]Participants (n=50, 25/group) with peripheral arterial disease will be randomly assigned to receive daily food item(s) containing traditional canola oil or an oil mixture representing the Western diet. Assessment of cognitive function will occur at baseline and at the end of the 8-week study schedule.
- 4. To assess compliance and tolerability through subjective feedback provided from participants during the chronic 8-week study. [ Time Frame: baseline at at 8 weeks ]Participants (n=50, 25/group) with peripheral arterial disease will be randomly assigned to receive a daily food item(s) containing traditional canola oil or an oil mixture representing the Western diet. Compliance and tolerability with food consumption (including side effects) will be assessed from participants' experiences throughout the 8-week study schedule.

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Ages Eligible for Study: | 40 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:Healthy age-matched participants (acute phase of the study):
- Healthy volunteers, male or female, > 40 years of age;
- Body Mass Index 18-30;
- Glycated hemoglobin <6.5%;
- Fasting serum total cholesterol <4 mmol/L and triglycerides <2.5 mmol/L;
- Blood pressure <140/90 mm Hg;
- Ankle-brachial index of >0.9;
- Willing to comply with the protocol requirements;
- Willing to provide informed consent;
- Participants having completed another food-related study are eligible to participate if it has been more than 3 months since their participation.
Inclusion criteria, peripheral arterial disease participants (acute and chronic phases of the study):
- Male or female, > 40 years of age;
- Documented peripheral arterial disease including those with claudication as defined by an ankle brachial index of ≤0.90 or asymptomatic carotid stenosis of >50%; or who have had a previous intervention for peripheral arterial disease;
- Stable medication profile for the past 3 months with no changes anticipated for the duration of the acute or chronic phases;
- Willing to comply with the protocol requirements;
- Willing to provide informed consent;
- Participants having completed another food study are eligible to participate if it has been more than 3 months since the study was completed.
Exclusion criteria, healthy age-matched participants (acute phase of the study):
- Currently smoking, or smoking within the last 6 months (Note: cigar smoking on an occasional basis will be permitted);
- Presence of a clinically diagnosed disease affecting the heart, liver, kidneys, lungs,gastrointestinal, endocrine or blood/immune systems that requires medical treatment;
- Taking any prescribed medication within the last 3 months with the exception of anti-depressants, birth control and hormone (estrogen) replacement therapy;
- Pregnancy;
- Amputation of upper or lower extremity on both sides;
- Has undergone a surgical procedure requiring local or general anesthetic within the last 3 months;
- History of gastrointestinal reactions or allergies to dietary oils and other ingredients in banana bread such as wheat and eggs;
- Daily consumption of omega-3 supplements.
Exclusion Criteria, Peripheral arterial disease participants (acute and chronic phases of the study):
- Currently smoking, or smoking within the last 6 months (Note: cigar smoking on an occasional basis will be permitted);
- Renal failure requiring dialysis;
- Ongoing cardiovascular event (e.g. angina)or medical illness within the last 3 months;
- Hormone (estrogen) replacement therapy;
- Amputation of leg, foot, arm or hand; post mastectomy or post lymphadenectomy;
- History of gastrointestinal reactions or allergies to dietary oils:for the acute study, to ingredients in banana bread such as wheat and eggs, ang for the chronic study, to one or more ingredients in the study foods which significantly limits the number of study foods that can be consumed;
- Inability to adhere to a regular diet;
- Daily consumption of omega-3 supplements.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01250275
Canada, Manitoba | |
IH Asper Clinical Research Insitute, St. Boniface General Hospital | |
Winnipeg, Manitoba, Canada |
Principal Investigator: | Carla Taylor, PhD | University of Manitoba |
Responsible Party: | Dr. Carla Taylor, Professor, Department of Human Nutritional Sciences, University of Manitoba |
ClinicalTrials.gov Identifier: | NCT01250275 |
Other Study ID Numbers: |
B2010:125 |
First Posted: | November 30, 2010 Key Record Dates |
Last Update Posted: | March 27, 2013 |
Last Verified: | March 2013 |
Canola Oil Peripheral Arterial Disease Peripheral Vascular Disease PAD |
Peripheral Arterial Disease Peripheral Vascular Diseases Atherosclerosis Arteriosclerosis |
Arterial Occlusive Diseases Vascular Diseases Cardiovascular Diseases |