Prospective, single-center, open clinical study to compare two methods (transesophageal echocardiography (TOE), Electric Kardiometrie®) to determine the contractility of the heart in adult patients undergoing cardiac surgical intervention.
Not Applicable
- Conditions
- I97Postprocedural disorders of circulatory system, not elsewhere classified
- Registration Number
- DRKS00005583
- Lead Sponsor
- Klinik für Anästhesiologie, operative Intensivmedizin und SchmerztherapieHelios Klinikum Krefeld
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Planned determining the contractility of the heart in adult patients undergoing cardiac surgical intervention.
• Preoperative examination of the heart of the patient before cardiac surgical intervention.
• Written informed consent of the patient to participate.
• Age> 18 years of age.
Exclusion Criteria
• ASA> 4 or life expectancy of the test subscriber is less than the test duration.
• Participation in another interventional clinical trials.
• diseases or disorders that participation in this clinical trial rule by investigator judgment (eg located in operational support systems (IABP, MECC), hemodynamic instability, heart valve diseases).
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Difference between the index of myokardial contractility measured with the compared measurement method (electric Kardiometrie®) and the value determined by means of TEE.
- Secondary Outcome Measures
Name Time Method • time required from the beginning of the establishment of the measurement procedures pending first readings.<br>• complication of the measurement method used.