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Clinical Trial

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

NCT: NCT04445909 · RECRUITING

NCT IDNCT04445909
StatusRECRUITING
Start Date2019-11-18
Completion2026-12-31
SponsorMedical University of Vienna (OTHER)
First posted
Last updated

Brief Summary

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.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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