Evaluation of CNAP During Anesthesia
Terminated
- Conditions
- General Anesthesia
- Registration Number
- NCT01032226
- Lead Sponsor
- Hopital Foch
- Brief Summary
The purpose of this study is to compare
* the non invasive measurement of arterial pressure (CNAP monitor)
* with the invasive measurement of arterial pressure (radial artery catheter) during induction and maintenance of general anesthesia
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 45
Inclusion Criteria
- Age >18
- ASA II, III or IV
- weight between 40 and 180 kg; BMI < 35
- surgical procedure performed in supine position
- normal Allen's test and hand Doppler examination.
Exclusion Criteria
- cardiac arrhythmias,
- history of vascular surgery or vascular implant in the upper limb
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison between both methods of arterial pressure measurement intraoperative
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms underlying CNAP's non-invasive arterial pressure measurement during anesthesia?
How does CNAP compare to radial artery catheters in accuracy for blood pressure monitoring under general anesthesia?
Are there specific biomarkers that influence the effectiveness of non-invasive versus invasive blood pressure monitoring in surgical patients?
What adverse events are associated with CNAP technology versus radial artery catheterization in anesthetized patients?
What alternative non-invasive hemodynamic monitoring technologies are being evaluated alongside CNAP for use during general anesthesia?
Trial Locations
- Locations (1)
Hôpital Foch
🇫🇷Suresnes, France
Hôpital Foch🇫🇷Suresnes, France