Ischemic Heart Disease Clinical Trial
Official title:
The Diagnostic Benefits of HyperQTM vs. Conventional ECG During Stress Test. A Comparison Study in Women Referred to Angiography.
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.
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 |
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Diagnostic
Country | Name | City | State |
---|---|---|---|
Israel | Shaare Zedek Medical Center | Jerusalem |
Lead Sponsor | Collaborator |
---|---|
BSP Biological Signal Processing Ltd. |
Israel,
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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