Magnetic Resonance Imaging of Vascular Function

July 31, 2014 updated by: Dr. Alan Moody, Sunnybrook Health Sciences Centre

A major function of blood vessels is to control blood flow by dilating or constricting depending on the demand. Vascular dysfunction is a state in which blood vessels fail to carry out its normal roles such as regulating blood flow. Diabetes is a risk factor for vascular dysfunction. Dysfunction may involve the smaller and/or larger blood vessels. Failure in the ability of large (conduit) blood vessels to control blood flow may be an early feature of atherosclerosis, a leading cause of stroke and heart attack. Measures of blood vessel dilation give an indication of the health of the vessel. Ultrasound and MRI can assess vascular function by measuring changes in blood vessel dilation. Diabetes may also affect tiny vessels in the kidney. These vessels become porous allowing albumin (a protein in the blood) to leak into the urine. The investigators can easily measure the presence of albumin in the urine.

This study aims to explore if MRI can demonstrate an association between vascular health in tiny and larger (conduit) blood vessels, by testing for an association between blood flow regulatory capacity of large vessels and presence of albumin in the urine.

Study Overview

Status

Unknown

Study Type

Observational

Enrollment (Anticipated)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Ontario
      • Toronto, Ontario, Canada, M5B 1W8
        • St Michael's Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Men and women with type 2 diabetes

Description

Inclusion Criteria:

  • Men and women with type 2 diabetes who:

    • are treated with oral hypoglycemic agents at a stable dose for at least 8 weeks
    • have diabetes diagnosed >6 months
    • have maintained stable weight for 2 months (within 3%)
    • have a valid Ontario Health Insurance Plan (OHIP) card and a family physician
    • if prescribed lipid medication, have taken a stable dose for at least 2 weeks
    • if prescribed blood pressure medication, have taken a stable dose for at least 1 week
    • can keep written food records
    • carotid intima-media thickness (cIMT) < 1.2 mm and ankle brachial index (ABI) of >0.9.

Exclusion Criteria:

  • Individuals who

    • take insulin
    • take steroids
    • have GI disease (gastroparesis, celiac disease, ulcerative colitis, Crohn's Disease, IBS)
    • have had a major cardiovascular event (stroke or myocardial infarction) in the past 6 months
    • take warfarin (Coumadin)
    • have had major surgery in the past 6 months
    • have a major debilitating disorder
    • have clinically significant liver disease ( liver transaminase levels > 130 U/L), excluding Nonalcoholic fatty liver (NAFL) disease or NASH
    • have hepatitis B or C
    • have renal failure (high creatinine > 150 mmol/L)
    • have serum triglycerides ≥ 6.0 mmol/L
    • have a history of cancer, except non-melanoma skin cancer (basal cell, squamous cell)
    • have food allergies to study food components
    • have acute or chronic infections (bacterial or viral)
    • have chronic inflammatory diseases (e.g. rheumatoid arthritis, lupus; ulcerative colitis)
    • have other conditions which in the opinion of any of the investigators would make them unsuitable for the study
    • Any condition or circumstance which would prevent an individual from having an MRI (e.g. individuals with prostheses or metal implants, or those who are excessively claustrophobic)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Popliteal FMD MRI technique correlates with albuminuria in those with early diabetic disease
Time Frame: One year
If this MRI technique is sensitive enough to demonstrate an association between flow mediated dilatation (FMD) of the popliteal artery and albuminuria, this will make a case for the use of the MRI technique in measuring effects of various interventions on vascular function.
One year

Secondary Outcome Measures

Outcome Measure
Time Frame
Blood measures related to cardiovascular disease and renal function
Time Frame: One year
One year
Dietary risk factors related to chronic disease
Time Frame: One year
One year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Alan Moody, DR, Sunnybrook Health Sciences Center
  • Principal Investigator: David Jenkins, DR, Unity Health Toronto

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2014

Primary Completion (Anticipated)

November 1, 2015

Study Registration Dates

First Submitted

July 30, 2014

First Submitted That Met QC Criteria

July 31, 2014

First Posted (Estimate)

August 1, 2014

Study Record Updates

Last Update Posted (Estimate)

August 1, 2014

Last Update Submitted That Met QC Criteria

July 31, 2014

Last Verified

July 1, 2014

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Diabetes

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