Performance Evaluation of the ViTrack Continuous Non-invasive Blood Pressure Measurement Device
Purpose
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.
Condition
- Blood Pressure
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- scheduled to undergo noncardiac surgery with general or spinal anesthesia - clinical indication for invasive intra-arterial pressure monitoring - palpable pulse
Exclusion Criteria
- difference of greater than 10 mmHg in the left versus right arm oscillometric systolic blood pressure - Upper extremity arteriovenous hemodialysis shunt - Upper extremity amputation - Planned surgical position/draping that precludes 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 the clinical team or study investigators
Study Design
- Phase
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
| ViTrack device |
|
Recruiting Locations
The University of Texas Health Science Center at Houston
Houston, Texas 77030
Houston, Texas 77030
More Details
- Status
- Recruiting
- Sponsor
- The University of Texas Health Science Center, Houston