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Performance Evaluation of the ViTrack Continuous Non-invasive Blood Pressure Measurement Device

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Not yet enrolling

Conditions

Blood Pressure

Treatments

Device: ViTrack device

Study type

Observational

Funder types

Other

Identifiers

NCT06719518
HSC-MS-24-0970

Details and patient eligibility

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.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

40 participants in 1 patient group

ViTrack device
Treatment:
Device: ViTrack device

Trial contacts and locations

1

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Central trial contact

Mohammad Khudirat; Mehmet Turan, MD

Data sourced from clinicaltrials.gov

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