Evaluation of Nexfin During Anesthesia and in Intensive Care (NexfinEval)
Completed
- Conditions
- Anesthesia
- Interventions
- Device: arterial pressure measurement (Nexfin, a noninvasive finger cuff system)
- Registration Number
- NCT01658631
- Lead Sponsor
- Hopital Foch
- Brief Summary
The purpose of this study is to compare the non invasive measurement of arterial pressure (Nexfin monitor)with the invasive measurement of arterial pressure (radial artery catheter)
* during induction of general anesthesia,
* during a leg raising test in the Intensive Care Unit
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 97
Inclusion Criteria
- Age >18
- ASA II, III or IV
- weight between 40 and 180 kg; BMI < 35
- normal Allen's test and/or hand Doppler examination.
Read More
Exclusion Criteria
- cardiac arrhythmias,
- history of vascular surgery or vascular implant in the upper limb
- Raynaud disease
Read More
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Intensive Care Unit patients arterial pressure measurement (Nexfin, a noninvasive finger cuff system) Arterial pressure measurement using Nexfin (a noninvasive finger cuff system) during a passive legs raising test Anesthesia arterial pressure measurement (Nexfin, a noninvasive finger cuff system) Arterial pressure measurement using Nexfin (a noninvasive finger cuff system) during the induction of anesthesia
- Primary Outcome Measures
Name Time Method Arterial pressure measurement Blood pressure will be followed for the duration of induction of anesthesia, an expected average of 20 minutes, or for the passive legs raising test, an expected average of 20 minutes
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
Institut Mutualiste Montsouris
🇫🇷Paris, France
Hopital Foch
🇫🇷Suresnes, France