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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00850486
Other study ID # SHZ_02
Secondary ID
Status Recruiting
Phase Phase 4
First received February 24, 2009
Last updated February 24, 2009
Start date August 2008
Est. completion date March 2010

Study information

Verified date February 2009
Source BSP Biological Signal Processing Ltd.
Contact David Rosenmann, MD
Phone 972-2-6555974
Email rosenmann@szmc.org.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

The purpose of this study is to verify the efficiency of the HyperQ technology compared with standard ECG analysis in detecting exercise induced ischemia in women who are referred to coronary angiography.


Description:

Cardiovascular disease (CVD) is the leading cause of mortality in women. In fact, CVD is responsible for a third of all deaths of women worldwide and half of all deaths of women over 50 years of age in developing countries. Historically, women have been underrepresented in clinical trials. The lack of good trial evidence concerning sex-specific outcomes has led to assumptions about CVD treatment in women, which in turn may have resulted in inadequate diagnoses and suboptimal management, greatly affecting outcomes. This knowledge gap may also explain why cardiovascular health in women is not improving as fast as that of men. Over the last decades, mortality rates in men have steadily declined, while those in women remained stable.

The treadmill exercise test is the classic initial investigation for the diagnosis of coronary artery disease (CAD), and significant ST depression on the ECG is the commonly used indicator of a positive test. Compared with men, in women it is known that ST depression is less likely to be associated with CAD. False positive rates of treadmill exercise testing have been reported to be as high as 67%, while positive predictive value is around 48-50%.

Coronary angiography is one of the most frequently performed procedures in women; however, non-obstructive (ie, <50% stenosis) CAD is frequently reported. Additionally, approximately 30% of women undergoing PTCA because of a positive exercise test are found to have normal coronary arteries. A successful outcome in the current study will significantly improve non-invasive diagnosis of CAD in women and may reduce the number of unnecessary invasive procedures performed.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date March 2010
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- A woman who was referred to angiography.

- A woman who is able (i.e. no contraindications) to perform an exercise stress test

- A woman who signed an informed consent form.

Exclusion Criteria:

- Contraindications for an exercise test

- Wolff-Parkinson-White (pre-excitation) syndrome.

- Left Bundle branch block, Complete Right bundle branch block or QRS duration > 120 ms, change in QRS morphology during exercise

- Atrial Fibrillation or significant ventricular arrhythmia

- Treatment with Digoxin

- Pacemaker

- Having taken beta blockers within 24 hours before the exercise test

- Pregnancy or suspected pregnancy

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Diagnostic


Intervention

Device:
Exercise test with HyperQ technology
High frequency components of the QRS complex within the ECG signal are analyzed off-line to provide an indication of ischemia induced depolarization abnormalities

Locations

Country Name City State
Israel Shaare Zedek Medical Center Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
BSP Biological Signal Processing Ltd.

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary HyperQ results from the exercise test vs. angiography results every 25 patients No
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