Coronary Artery Disease Clinical Trial
Official title:
Do Innovative Strategies Complement Medical Management to Reduce Cardiovascular Risk Factors Following Coronary Artery Bypass Graft Surgery?
Verified date | February 2009 |
Source | St. Michael's Hospital, Toronto |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Ethics Review Committee |
Study type | Interventional |
Background: Treatment targets for cardiac risk factor reduction are not being met.
Therefore, there is a need for new strategies to assist patients in meeting these goals.
Objective: To determine the amount of any additional benefit on risk factor reduction
associated with the consumption of the "dietary portfolio" (a low fat diet with soy, nuts
and viscous fibres), above that achieved with medical management in diabetic patients
following cardiac surgery.
Description: 35 cardiac surgery patients with diabetes will be instructed on how to
incorporate the dietary portfolio foods into their diet for four weeks. Changes in blood
cholesterol, markers of inflammation, blood sugar control and modifiable risk factors will
be assessed after 2 and 4 weeks of therapy.
Relevance: Maximizing cardiac risk factor reduction through a combined approach (dietary
plus medication) should improve outcomes, reduce rates of re-hospitalization and improve
quality of life in diabetic patients after heart surgery.
Status | Completed |
Enrollment | 35 |
Est. completion date | May 2010 |
Est. primary completion date | December 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Patients with type II diabetes mellitus 2. Recently (<5 months) undergone coronary artery bypass graft surgery 3. Taking cholesterol lowering medication Exclusion Criteria: 1. Can not speak English and have no available interpreter 2. Refuse Informed Consent 3. Had "off pump" CABG 4. Are intolerant of statins 5. Are pre-menopausal (women) or are on HRT 6. Have serious concomitant disease 7. Take insulin 8. Are <18 years of age 9. receive incomplete revascularization 10. documented history of drug or alcohol abuse 11. Intend to become pregnant during study period 12. Have an unreliable psychological condition that makes them unlikely to comply |
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
Canada | St. Michael's Hospital | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
St. Michael's Hospital, Toronto | Canadian Diabetes Association |
Canada,
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* Note: There are 41 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Primary Outcome: Reduction of total and LDL cholesterol | baseline to 4 weeks | No | |
Secondary | Improvement in endothelial function and EPC counts | Baseline to 4 weeks | No | |
Secondary | Reduction in CRP | baseline to 4 weeks | No | |
Secondary | Feasibility and tolerability | Baseline to 4 Weeks | No | |
Secondary | Reduction in markers of inflammation ie TNF, IL-6 | Baseline to 4 weeks | No | |
Secondary | Improved markers of glycemic control - fructosamine, HOMA | baseline to 4 weeks | No |
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