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Sponsors and Collaborators: |
University Hospital Inselspital, Berne Edwards Lifesciences |
Information provided by: | University Hospital Inselspital, Berne |
ClinicalTrials.gov Identifier: | NCT00583687 |
The purpose of this study is to compare changes of minimally invasive arterial pulse contour cardiac output with changes of intermittent and continuous thermodilution cardiac output by pulmonary artery catheter in hemodynamic unstable patients with rapid changing vascular tone (changing dosage of vasoactive drugs or inotropics, or volume challenge). Simultaneously, global parameters of oxygen delivery and consumption will be compared with regional flow parameters and tissue oxymetry (near infrared spectrometry and laser-Doppler). While continuous thermodilution cardiac output is used for patient management, pulse contour cardiac output, intermittent thermodilution cardiac output and tissue oxymetry is only used for monitoring.
Condition | Intervention |
Cardiac Output, High Cardiac Output, Low Vasodilation Vasoconstriction Hemodynamics |
Device: Vigileo TM / Flotrac TM (Minimally invasive cardiac output system consisting of arterial line sensor and cardiac output monitor) Other: Passive leg raising Other: Volume challenge / Change of vasoactive drugs or inotropics Device: Inspectra TM/O-To-See TM (Tissue oxymetry with near infrared spectroscopy and laser-Doppler) |
MedlinePlus related topics: | Heart Failure |
Study Type: | Interventional |
Study Design: | Treatment, Open Label, Single Group Assignment |
Official Title: | Pulse Contour Analysis and Tissue Oxymetry in Changing Vascular Tone |
Estimated Enrollment: | 30 |
Study Start Date: | December 2007 |
Estimated Study Completion Date: | December 2008 |
Estimated Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Christoph C Ganter, M.D. | 0041-31-632 01 67 | christoph.ganter@insel.ch |
Switzerland | |||||
Department of Intensive Care Medicine, University Hospital Inselspital, Berne | Recruiting | ||||
Bern, Switzerland, 3010 | |||||
Contact: Christoph C Ganter, M.D. 0041-31-632 01 67 christoph.ganter@insel.ch | |||||
Principal Investigator: Christoph C Ganter, M.D. |
University Hospital Inselspital, Berne |
Edwards Lifesciences |
Principal Investigator: | Christoph C Ganter, M.D. | Department of Intensive Care Medicine, University Hospital, Inselspital, Berne |
Responsible Party: | Departement of Intensive Care Medicine, University Hospital Inselspital, Berne ( Christoph C Ganter, MD ) |
Study ID Numbers: | KEK-3107-UHB-1316 |
First Received: | December 18, 2007 |
Last Updated: | June 2, 2008 |
ClinicalTrials.gov Identifier: | NCT00583687 |
Health Authority: | Switzerland: Ethikkommision |
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