The Continuity Study

Recruiting N/A Interventional Study
Blood Pressure
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
188 (estimated)
Sponsor
Becton, Dickinson and Company · Industry
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About This Trial

A before and after interventional cohort study comparing intermittent blood pressure measurement using the oscillometric arm cuff to continuous noninvasive blood pressure (cNIBP) measurement using the VitaWave finger cuffs in subjects undergoing elective surgery in an outpatient setting.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Signed informed consent 2. Age ≥ 18 years 3. American Society of Anesthesiologists (ASA) Physical Status ≥ 2 4. Scheduled for elective noncardiac surgery with intermittent arterial blood pressure monitoring using oscillometric arm cuff Exclusion Criteria: 1. Patient who is …
Contacts

Cristina Johnson

949-308-5850

APMContinuity.Study@bd.com

CONTACT