Actively Recruiting
Performance Evaluation of the ViTrack Continuous Non-invasive Blood Pressure Measurement Device
Led by The University of Texas Health Science Center, Houston · Updated on 2026-02-27
40
Participants Needed
1
Research Sites
32 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to calibrate the ViTrack™ arterial pressure waveform against intra-arterial pressure (IAP) in dynamic clinical settings and to assess the optimized ViTrack™ design to measure and continuously track blood pressure over a wide, clinically-relevant pressure range.
CONDITIONS
Official Title
Performance Evaluation of the ViTrack Continuous Non-invasive Blood Pressure Measurement Device
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Scheduled to undergo noncardiac surgery with general or spinal anesthesia
- Clinical indication for invasive intra-arterial pressure monitoring
- Palpable pulse
You will not qualify if you...
- Difference greater than 10 mmHg between left and right arm oscillometric systolic blood pressure
- Upper extremity arteriovenous hemodialysis shunt
- Upper extremity amputation
- Planned surgical position or draping that prevents access to the wrist
- Wrist distortion or pain from arthritis
- Prior trauma or surgery at the radial artery monitoring site
- Unable to provide informed consent
- Clinical contraindication as determined by clinical team or study investigators
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of Texas Health Science Center at Houston
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
M
Mehmet Turan, MD
CONTACT
M
Mohammad Khudirat
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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