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Completed

NCT Number: NCT01256320

Egg Study With Peripheral Arterial Disease

The current research study has the potential to generate data that would provide solid clinical endpoints as to the impact of including eggs in a regular diet in individuals with peripheral arterial disease. Any one of three potential outcomes may be observed as a result of this study, and they are predicted as follows: 1) Egg consumption does not lead to a deterioration of indices of cardiovascular health; 2) Egg consumption improves indices of cardiovascular health; 3) Egg consumption worsens the indices of cardiovascular health.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

IH Asper Clinical Research Institute, St. Boniface General Hospital

Winnipeg, Manitoba, R2H 2A6, Canada

About this study

Given the hypotheses proposed, if either of the first two predictions prove to be positive, they will help encourage directive efforts to be made toward effective nutrition messages for egg consumption in the peripheral arterial disease and the healthy population. If the last prediction is positive, while least favourable, it will still establish important information to assist the industry in their efforts toward establishing population-specific nutrition messaging.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Presence of 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;
  • Male or female, > 40 years of age;
  • Willing to comply with the protocol requirements;
  • Willing to provide informed consent;
  • Stable medication profile with no changes anticipated for the duration of the proposed study schedule (8 weeks);
  • Participants having completed the Flax Study are eligible to participate if their completion has been more than 3 months.

Exclusion criteria

  • Renal failure requiring dialysis;
  • Diabetes, requiring diabetic medication; Participants with diabetes who do not require diabetic medication and have good glycemic control will be eligible for participation in the study. Participant with elevated fasting blood glucose levels and glycated hemoglobin above 'standard of care' at baseline will not proceed with the study;
  • Hyperlipidemia as defined by a cholesterol of >4.1 mmol/L (as per the National Cholesterol Education Program Adult Treatment Panel III, (NCEP ATP III) guidelines;
  • Hormone replacement therapy;
  • Inability to adhere to a regular diet;
  • Habitual egg intake of 5 or more eggs per week;
  • History of gastrointestinal reactions or allergies to eggs;
  • Daily consumption of omega-3 supplements.

Treatment and study plan

Classic Egg Group

Other

consumption of 6 eggs/week (1 egg/day for 6 days with 1 day rest) of commercial classic eggs

Omega 3 Egg Group

Other

consumption of 6 eggs/week (1 egg/day for 6 days with 1 day rest) of commercial Omega-3 eggs

Primary outcomes

  1. Establish quantitative and qualitative data on the dietary patterns, including egg consumption, in patients with PAD

    Time frame: change in assessments from baseline to 8 weeks

    The following assessments are included to measure the primary outcome:

    1)Anthropometrics: weight, height; waist circumference, Body Mass Index; 2)Dietary Assessment:3-day dietary food record, food frequency questionnaire (baseline only); 3)Biochemical Analyses; 4)Expression and Metabolic Profiling; 5)Arterial Compliance: Ankle-brachial index, pulse wave velocity, arterial vasodilation, and advanced glycation endproducts; 6) Semi-structured interview.

Secondary outcomes

  1. Determine the impact of consuming 6 eggs per week on primary end-points and other modifiable risk factors in patients with PAD.

    Time frame: change in assessments from baseline to 8 weeks

    The following assessments are included to measure the primary outcome:

    1)Anthropometrics: weight, height; waist circumference, Body Mass Index; 2)Dietary Assessment:3-day dietary food record, food frequency questionnaire (baseline only); 3)Biochemical Analyses; 4)Expression and Metabolic Profiling; 5)Arterial Compliance: Ankle-brachial index, pulse wave velocity, arterial vasodilation, and advanced glycation endproducts; 6) Semi-structured interview.

Sponsors and collaborators

Lead sponsor

University of Manitoba

Other

Registry information

Official study title

The Impact of Egg Consumption on Indices of Vascular Health in Individuals With Peripheral Arterial Disease

Important dates

Study start
2010
Primary completion
2012
Study completion
2013
First posted
Dec 8, 2010
Registry last updated
May 4, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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