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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 arterial waveform analysis in the radial artery. 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®). The continuous monitoring of blood pressure by this technique 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 arterial waveform analysis in the radial artery by Pulsioflex® in major surgery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02717468
Study type Interventional
Source Poitiers University Hospital
Contact
Status Completed
Phase N/A
Start date February 2016
Completion date February 2017

See also
  Status Clinical Trial Phase
Completed NCT02941952 - Comparative Noninvasive Continuous Cardiac Output by the Clearsight® With Invasive Monitoring by PICCO® in Abdominal Major Surgery N/A
Completed NCT01678950 - MostCare Versus Echo-Doppler for Cardiac Output Measurement N/A
Recruiting NCT05754489 - Exercise Oxygen Kinetic and Cardiac Output in Hypertrophic Cardiomyopathy