Prospective Validation of Intraoperative Blood Pressure Monitors
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCiusss de L'Est de l'Île de Montréal
About this trial
This observational study aims to identify the incidence and importance of discrepancies between measurements of intraoperative invasive and noninvasive blood pressure monitoring in patients undergoing non-cardiac surgeries under general anesthesia . The main questions it aims to answer are :
* The importance of the differences, in mmHg, between the non-invasive and invasive blood pressure measurements (NIBP-IBP) on systolic, diastolic and mean arterial pressure. * Identify the predictive factors associated with these differences.
Eligibility criteria
Qualifiers
Fully consented, adult patients above 18 years old;
Undergoing surgery of duration time expected at least 60 minutes using general anesthesia;
Supine positioning during the surgery;
Surgery requiring an arterial line;
Disqualifiers
Atrial fibrillation, multifocal atrial tachycardia, or any other irregular hear rythm;
Gradient of mean arterial pressure between the two arms greater than 5 mm Hg, as measured during the recruitment process.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Source ClinicalTrials.gov