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Primary Care Audit of Global Risk Management

Primary Care Audit of Global Risk Management

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00950703
Acronym
PARADIGM
Enrollment
3015
Registered
2009-08-03
Start date
2009-03-31
Completion date
2015-09-30
Last updated
2015-10-14

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

Conditions

Cardiovascular Diseases

Keywords

Assessing the perceptions of Canadian Primary care physicians towards global Cardiovascular risk assessment.

Brief summary

1. Assessing the perception of Canadian Primary Care Physicians towards global cardiovascular risk assessment. 2. Correlating physician perceptions to actual practice data, gathered via a retrospective chart audit. 3. Evaluating the impact of a prospective educational and peer-practice pattern intervention on future assessment o cardiovascular risk and 4. Assessing the role of carotid atherosclerosis assessment(Carotid IMT and plaque) as an adjunct to global risk prediction.

Detailed description

The majority of cardiovascular events occur in people with low to intermediate Framingham Risk Score. Despite evidence-based guidelines, the appropriate use of lipid-lowering therapies in this population remains limited and controversial. Strategies to refine risk stratification in primary prevention have been poorly adopted. Dissemination of practice-changing trials and closing the care gap in primary care remain a priority and a challenge. Considerable confusion remains regarding the optimal application of lipid-lowering therapy in primary prevention. Importantly, it remains largely unknown which tools or techniques are used by Canadian primary care physicians to identify global vascular risk, and what barriers exist to implementing risk reduction therapies in such individuals. For primary prevention of patients with normal levels of LDL-Cholesterol who are at increased risk on the basis of elevated hsCRP, it remains unproven whether statin therapy will effectively reduce vascular event rates. The JUPITER trial was launched in 2003 comparing rosuvastatin with placebo in 18,000 primary prevention patients with LDL-cholesterol of less than 3.36mM who also have an hsCRP of greater than 2 mg/L. This trial has been stopped early due to unequivocal morbidity and mortality benefits in favor of the treatment strategy, and the final results will be available in early November, 2008. JUPITER, once published, will require a major change in physician behavior with respect to screening and treating cardiovascular risk.

Interventions

None listed

Sponsors

AstraZeneca
CollaboratorINDUSTRY
Canadian Collaborative Research Network
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Men more than or equal to 40 yrs old and women more than or equal to 50 yrs old; 2. No previous history of atherosclerosis( angina, TIA, myocardial infarction, stroke, peripheral arterial disease); 3. Non-diabetic; 4. Absence of lipid lowering treatment (current or past).

Exclusion criteria

1. Known history of atherosclerosis or diabetes; 2. Use of lipid lowering therapies (statins, ezetimibe, fibrates, niacin, fish oil); 3. Use of postmenopausal hormone replacement therapy; 4. Use of immunosuppressant's or steroids; 5. Active liver disease or hepatic dysfunction(ALT\>2times the ULN); 6. Active renal disease (baseline Creatinine \>170 umol/L); 7. History of malignancy within the past 5-years; 8. Chronic inflammatory conditions such as arthritis, lupus or inflammatory bowel disease; 9. Known alcohol or drug abuse; 10. Failure to provide informed consent.

Design outcomes

Primary

MeasureTime frame
The Primary objective of the PARADIGM study is to evaluate the impact of an educational and peer-practice pattern intervention on primary care physician behavior towards global cardiovascular risk prediction in otherwise healthy individuals.1 year

Secondary

MeasureTime frame
Evaluate the prevalence of classic and novel markers of risk (hsCRP and ApoB/ApoA1).1 year
Evaluate within a sub-study, the feasibility of carotid atherosclerosis assessment.1 year

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026