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

Part of paid clinical trials in Houston, Texas.

Sponsor
The University of Texas Health Science Center, Houston
Study ID
NCT06719518
Status
Recruiting
Apply to this trial

Conditions

  • Blood Pressure

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • ViTrack device — 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 Details

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.

Key Dates

Start date
Dec 17, 2025
Status verified
Feb 2026
Primary completion
Jul 31, 2026
Completion
Jul 31, 2026

Study Design

Enrollment
40 participants (estimated)

Arms

  • Arm: ViTrack device

Primary Outcome Measure

Comparison of Diastolic Blood Pressure [ Time Frame: From start of surgery up to 24 hours after surgery ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
The University of Texas Health Science Center at HoustonHoustonTexas77030
Mehmet Turan, MD
[email protected]
(713) 500-6251
Mohammad Khudirat
[email protected]
(713) 500-6200

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The University of Texas Health Science Center at Houston· Houston, TX

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