Status:
NOT_YET_RECRUITING
The Continuity Study
Lead Sponsor:
Edwards Lifesciences
Conditions:
Blood Pressure
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
A before \& after interventional cohort study comparing intermittent blood pressure measurement using the oscillometric arm cuff to continuous noninvasive blood pressure measurement using the VitaWave...
Eligibility Criteria
Inclusion
- Signed informed consent
- Age ≥ 18 years
- ASA Physical Status ≥ 2
- Scheduled for elective noncardiac surgery with intermittent arterial blood pressure monitoring using oscillometric arm cuff
Exclusion
- Patient who is known to be pregnant
- Patient with existing or planned arterial pressure catheter
- Patient in whom systolic arterial pressure differs by more than 20 mmHg between the right and left arms
- Inability to place oscillometric cuff on the subject's upper extremity
- 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
- Finger or hand deformity that prevents proper placement of finger cuff by visual inspection
- Inability to place finger cuffs due to subject anatomy, condition, or obstructive paraphernalia (such as false nails)
Key Trial Info
Start Date :
November 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2026
Estimated Enrollment :
188 Patients enrolled
Trial Details
Trial ID
NCT07216573
Start Date
November 1 2025
End Date
December 1 2026
Last Update
October 14 2025
Active Locations (1)
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1
University of Rochester Medical Center
Rochester, New York, United States, 14620