Skip to content

Alternative Risk Markers in Coronary Artery Disease (ARMCAD)

Correlation of Multiple Risk Factors With Presence and Severity of Coronary Artery Disease.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00403351
Enrollment
665
Registered
2006-11-23
Start date
2006-10-31
Completion date
2016-05-31
Last updated
2020-09-02

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

Conditions

Coronary Artery Disease

Keywords

Risk, Coronary artery disease, Heart Rate variability, Pulse wave analysis, BNP, CRP

Brief summary

Estimating the risk of future cardiovascular events such as death, stroke and myocardial infarction using traditional risk factors (such as age, gender, smoking, diabetes, hyperlipidaemia and hypertension) is well accepted in patients with and without existing cardiovascular disease. These estimates are based on a number of robust observational studies, including the original Framingham study. While these methods apply reasonably well on a population level their application to the individual patients is not always straightforward. In addition, risk charts, such as those published by the Joint British Societies and American Heart Association, may underestimate risk in certain groups, notably diabetics and patients of Indo-Asian background, whilst overestimating risk in others (by as much as 50% in some studies).

Detailed description

A number of variables including clinical, biochemical, and enzymatic have been evaluated to see if they add to conventional risk-reduction models such as Framingham and if so, to understand if they may be used in routine clinical practice. The aim of this study is to assess several known and a few novel risk-factors (heart rate variability, pulse wave analysis, high-sensitivity CRP and BNP) prior to planned elective coronary angiography (cross-sectional analysis) and in a prospective cohort of high and low-risk patients.

Interventions

None listed

Sponsors

Royal Brompton & Harefield NHS Foundation Trust
CollaboratorOTHER
IM Medical Ltd, Melbourne
CollaboratorUNKNOWN
Monash University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults (18 years or older) * Male or Female

Exclusion criteria

* Acute coronary syndrome * Urgent angiography * Assessment would constitute harm to patient * Informed consent not obtained

Design outcomes

Primary

MeasureTime frame
Extent and severity of angiographic coronary artery diseasecross-sectional
All-cause death or myocardial infarction1, 2, 5 years
All-cause death, MI or need for cardiac surgery1, 2, 5 years

Secondary

MeasureTime frame
All-cause death1, 2, 5 years

Other

MeasureTime frame
Other cardiovascular events or procedures1, 2, 5 years

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026