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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06719518

Enrollment

Registered

2024-12-05

Start date

2025-12-17

Completion date

2026-07-31

Last updated

2026-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Pressure

Keywords

ViTrack, blood pressure monitoring

Brief summary

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.

Interventions

DEVICEViTrack device

In the operating room the ViTrack™ device will be applied the wrist. Monitoring will start in the operating room and will continue throughout the surgery. The device can be worn on either wrist. It will be connected to a power unit that will capture blood pressure data and stream the data to a secure laptop

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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

Design outcomes

Primary

Measure	Time frame	Description
Comparison of Diastolic Blood Pressure	From start of surgery up to 24 hours after surgery	255 time points compared across continuous blood pressure (mmHg)
Comparison of Systolic Blood Pressure	From start of surgery up to 24 hours after surgery	255 time points compared across continuous blood pressure (mmHg)

Secondary

Measure	Time frame
Number of participants who show signs of Skin Irritation	From start of surgery up to 72 hours after surgery

Countries

United States

Contacts

CONTACTMehmet Turan, MD

Mehmet.A.Turan@uth.tmc.edu(713) 500-6251

CONTACTMohammad Khudirat

Mohammad.Khudirat@uth.tmc.edu(713) 500-5558

PRINCIPAL_INVESTIGATORMehmet Turan, MD

The University of Texas Health Science Center, Houston

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026