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The Continuity Study
Recruiting
Continuous Blood Pressure Monitoring During Outpatient Surgery
Who can join
Ages 18 and older · All sexes
Full 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 known to be pregnant 2. Patient with existing or planned arterial pressure catheter 3. Patient in whom systolic arterial pressure differs by more than 20 mmHg between the right and left arms 4. Inability to place oscillometric cuff on the subject's upper extremity 5. Extreme contraction of the smooth muscle in the arteries and arterioles of the lower arm and hand, such as may be present in patients with Raynaud's disease 6. Finger or hand deformity that prevents proper placement of finger cuff by visual inspection 7. Inability to place finger cuffs due to subject anatomy, condition, or obstructive paraphernalia (such as false nails)
About the 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.
What is being tested
- HemoSphere Vita Monitor with VitaWave or VitaWave Plus Finger Cuff Adult, and ForeSight Large Sensors (device)
Sponsor: Becton, Dickinson and Company · Participants: 188 · Started: May 7, 2026
Contact the study team
- Cristina Johnson · Phone: 949-308-5850
Official record on ClinicalTrials.gov — NCT07216573
Locations in the U.S.
| New York | University of Rochester Medical Center, Rochester |
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.