Actively Recruiting
The Continuity Study
Led by Edwards Lifesciences · Updated on 2026-04-22
188
Participants Needed
1
Research Sites
43 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
The Continuity Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent
- Age 18 years or older
- American Society of Anesthesiologists (ASA) Physical Status 2 or higher
- Scheduled for elective noncardiac surgery with intermittent blood pressure monitoring using an oscillometric arm cuff
You will not qualify if you...
- Known pregnancy
- Existing or planned arterial pressure catheter
- Systolic arterial pressure differs by more than 20 mmHg between right and left arms
- Unable to place oscillometric cuff on upper arm
- Severe contraction of smooth muscle in lower arm or hand (e.g., Raynaud's disease)
- Finger or hand deformity preventing proper finger cuff placement
- Inability to place finger cuffs due to anatomy, condition, or obstructive items (e.g., false nails)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Rochester Medical Center
Rochester, New York, United States, 14620
Actively Recruiting
Research Team
C
Cristina Johnson
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
OTHER
Number of Arms
2
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