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Clinical Trial Summary

In high-risk patients, it is now recommended to guide the intraoperative volume replacement via the stroke volume.

Today, the most commonly used technique for estimating the stroke volume is the transpulmonary thermodilution and the arterial waveform analysis in the radial artery by PICCO®.

This technique has the disadvantage of being invasive and increasing the time dedicated to anesthesia during the surgery.

The future is the non-invasive monitoring of stroke volume. Thus, Edwards Life Science has developed a continuous monitoring technology and non-invasive arterial pressure, cardiac output and stroke volume using a digital sensor (ClearSight®). This continuous monitoring of blood pressure was validated in cardiothoracic surgery but studies about monitoring cardiac output or stroke volume are inconclusive and contradictory.

The objective of this study is to compare the use of non-invasive monitoring of stroke volume by ClearSight® with the transpulmonary thermodilution and the arterial waveform analysis in radial artery by PICCO® in abdominal major surgery.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT02941952
Study type Interventional
Source Poitiers University Hospital
Contact
Status Completed
Phase N/A
Start date October 28, 2016
Completion date May 7, 2018

See also
  Status Clinical Trial Phase
Completed NCT01678950 - MostCare Versus Echo-Doppler for Cardiac Output Measurement N/A
Completed NCT02717468 - Comparative Noninvasive Continuous Cardiac Output by the Clearsight With Invasive Monitoring by Pulsioflex in Abdominal Surgery N/A
Recruiting NCT05754489 - Exercise Oxygen Kinetic and Cardiac Output in Hypertrophic Cardiomyopathy