Stroke Volume Analysis During Aortic Valve Replacement Trial (standart)
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Details and patient eligibility
About
Compromised peripheral tissue oxygenation during surgery may lead to worse patient outcome, mainly due to post-operative infections or heart failure. Insufficient stroke volume and/or cardiac output due to hypovolemia or cardiac defects play a central role in causing poor peripheral tissue oxygenation. In order to assess stroke volume, there are numerous invasive and non-invasive methods available. Up to the present date it is unknown, if these methods may by used interchangeably in patients with severe cardiac defects like aortic stenosis.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- scheduled transcatheter aortic valve implantation
- signed patient consent form
- aged 18 or older by time of surgery
- no participation in other clinical trials
Exclusion criteria
- pregnant or breast-feeding women
- emergency surgery
Trial design
68 participants in 2 patient groups
Trial contacts and locations
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Central trial contact
Michael Sander, MD
Data sourced from clinicaltrials.gov
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