Clinical Trials Directory

Trials / Completed

CompletedNCT03114579

Evaluation of the Measurement of Cardiac Output by the NEXFIN HD Monitor in Peroperative

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
42 (actual)
Sponsor
Centre Hospitalier Universitaire, Amiens · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Continuous perioperative cardiac output (DC) and blood pressure (PA) monitoring contributes to hemodynamic stability and ensures adequate perfusion pressure, resulting in a reduction in morbidity and mortality and length of hospital stay. The monitors usually used in perioperative are either semi-invasive and difficult for calibration (oesophageal Doppler) or invasive (arterial catheter). The Nexfin HD allows these two measurements and it is completely non-invasive, remains to validate its use in peroperative.

Conditions

Interventions

TypeNameDescription
DEVICEIntraoperative heart rate measurement (reference method)Measurement of cardiac output by both monitors: NEXFIN HD and oesophageal doppler, blood pressure measurement by the catheter and NEXFIN HD monitor, and cardiac output and blood pressure measurements after treatment administration (vasoconstrictor or filling)
DEVICENEXFIN HD

Timeline

Start date
2015-02-11
Primary completion
2017-02-11
Completion
2017-02-11
First posted
2017-04-14
Last updated
2017-04-14

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03114579. Inclusion in this directory is not an endorsement.