Clinical utility of the acoustic detection of coronary stenosis as early rule-out system –a blinded comparison to standard care
- Conditions
- I25.19
- Registration Number
- DRKS00016986
- Lead Sponsor
- Studienzentrum der Herzklinik Ulm
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 500
• Males and females, aged 40 years or above.
• Symptoms suggestive of stable CAD.
• Having indication for further evaluation of suspected CAD
• Have signed the informed consent form.
• Known CAD (previous myocardial infarction, angiographical CAD diagnosis and/or previous PCI and/or previous CABG)
• DF score>85%
• Acute Coronary syndrome
• Implanted donor heart, mechanical heart, mechanical heart pump.
• Pacemaker, Cardioverter Defibrillator (ICD) or other implanted electronic equipment in the area above and around the heart.
• Significant operation scars, abnormal body shape, fragile or compromised skin in the fourth left intercostal space recording area.
• Same day vaso-dilating drugs (e.g. nitroglycerine) prior to CAD-scoring.
• Missing informed consent
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method