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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00403351
Other study ID # CP-02/04
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2006
Est. completion date May 2016

Study information

Verified date September 2020
Source Monash University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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).


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.


Recruitment information / eligibility

Status Completed
Enrollment 665
Est. completion date May 2016
Est. primary completion date June 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Locations

Country Name City State
Australia Box Hill Hospital (Eastern Health) Box Hill Victoria
Australia Caulfield General Medical Centre Caulfield Victoria
Australia Northern Hospital (Northern Health) Epping Victoria
Australia Alfred Hospital Melbourne Victoria

Sponsors (3)

Lead Sponsor Collaborator
Monash University IM Medical Ltd, Melbourne, Royal Brompton & Harefield NHS Foundation Trust

Country where clinical trial is conducted

Australia, 

References & Publications (3)

Kotecha D, Flather M, McGrady M, Pepper J, New G, Krum H, Eccleston D. Contemporary predictors of coronary artery disease in patients referred for angiography. Eur J Cardiovasc Prev Rehabil. 2010 Jun;17(3):280-8. doi: 10.1097/HJR.0b013e3283310108. — View Citation

Kotecha D, New G, Collins P, Eccleston D, Krum H, Pepper J, Flather MD. Radial artery pulse wave analysis for non-invasive assessment of coronary artery disease. Int J Cardiol. 2013 Aug 10;167(3):917-24. doi: 10.1016/j.ijcard.2012.03.098. Epub 2012 Apr 4. — View Citation

Kotecha D, New G, Flather MD, Eccleston D, Pepper J, Krum H. Five-minute heart rate variability can predict obstructive angiographic coronary disease. Heart. 2012 Mar;98(5):395-401. doi: 10.1136/heartjnl-2011-300033. Epub 2011 Nov 25. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Other cardiovascular events or procedures 1, 2, 5 years
Primary Extent and severity of angiographic coronary artery disease cross-sectional
Primary All-cause death or myocardial infarction 1, 2, 5 years
Primary All-cause death, MI or need for cardiac surgery 1, 2, 5 years
Secondary All-cause death 1, 2, 5 years
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