Development und validation of a new approach for perioperative, non continuous, non-invasive measurement of blood pressure, pulse pressure variation and stroke volume in mechanically ventilated patients in patients undergoing cardiac surgery
Not Applicable
- Conditions
- blood pressure, stroke volume, stroke volume variation, pulse pressure Variation of patients unerrgoing cardiac surgery
- Registration Number
- DRKS00009546
- Lead Sponsor
- Klinik für Anästhesiologie mit Schwerpunkt operative Intensivmedizin, Campus Charite Mitte und Virchow Klinikum, Charite - Universitätsmedizin Berlin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 36
Inclusion Criteria
Informed consent from patient, age = 18 years, cardiac surgery, no paritcipation in a drug trial, surgery under general anesthesia
Exclusion Criteria
No informed consent, patients unable to consent, pergnant or breast feeding women, emergency surgery, side difference of blood pressure > 12 mmHg, tissue ischemia, Severe peripheral arterial vascular occlusion disease = 4 after Fontaine, atrial fibrillation, need of intra aortic balloon pump
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measurement of blood pressure (absolute and trending) by use of piezo-foil technology and invasively in the perioperative setting.
- Secondary Outcome Measures
Name Time Method Measurement of pulse pressure and stroke volume variation by use of piezo-foil technology and invasively in the perioperative setting.