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
| Type | Name | Description |
|---|---|---|
| DEVICE | Intraoperative 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) |
| DEVICE | NEXFIN 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.