Validation of Continuous Transcutaneous Carbon Dioxide Monitoring in VA-ECMO Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorMedical University of Vienna

About this trial

Carbon dioxide in patients on veno-arterial extracorporeal membrane oxygenation (VA-ECMO) is eliminated via respirator as well as via the oxygenator's membrane of the ECMO machine. Consequently, monitoring of end-tidal carbon dioxide tensions is limited, which can result in marked swings towards non-physiological values. Hyper- and hypocapnia, however, can have detrimental effects on organ perfusion in a great number of patients supported with VA-ECMO. Continuous, rapidly applicable monitoring of reliable carbon dioxide measures would therefore be extremely helpful to prevent harmful deviations from the norm. The investigators therefore try to assess the accuracy and the precision of continuously measured non-invasive transcutaneous carbon dioxide partial pressures when compared with tensions determined by blood gas analysis.

Eligibility criteria

Qualifiers

Low cardiac output requiring VA-ECMO support.

Disqualifiers

Age < 18 years

Trial design

Treatments tested in this trial

  • VA-ECMO

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators