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Study identifier: NCT07216573 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

The Continuity Study

Condition: Blood Pressure  ·  Sponsor: Becton, Dickinson and Company

PhaseNA
Planned participants188
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Cristina Johnson  ·  949-308-5850  ·  APMContinuity.Study@bd.com

Always discuss trial participation with your own doctor first.

Locations (1)

University of Rochester Medical CenterRochester, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07216573