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NCT06887465 | NOT YET RECRUITING | Blood Pressure


Non-invasive Blood Pressure Monitoring
Sponsor:

Vena Vitals

Brief Summary:

The goal of this observational study is to evaluate the accuracy and reliability of the VeriTrack non-invasive blood pressure monitor compared to radial arterial catheterization in adult surgical patients. The main question it aims to answer is: How well does VeriTrack measure continuous blood pressure compared to an arterial catheter? Researchers will compare VeriTrack readings to arterial line measurements to determine if the VeriTrack provides comparable accuracy and clinical utility. Participants will wear the VeriTrack device during surgery and have a radial arterial catheter placed as part of standard care.

Condition or disease

Blood Pressure

Intervention/treatment

Non-invasive Blood Pressure Monitor

Study Type : OBSERVATIONAL
Estimated Enrollment : 100 participants
Official Title : Comparison of Non-Invasive Wearable Sensors to Radial Arterial Catheterization on Human Subjects
Actual Study Start Date : 2025-06
Estimated Primary Completion Date : 2025-12
Estimated Study Completion Date : 2025-12

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Patients whose blood pressure will be monitored using an arterial line during their procedure
  • * Patients who have a palpable dorsalis pedis pulse
Exclusion Criteria
  • * Patients who have non-palpable dorsalis pedis pulses
  • * Patients whose limbs are inaccessible for placement of Vena Vitals Wearable
  • * Patients with known allergy to adhesives and/or silicone

Non-invasive Blood Pressure Monitoring

Location Details

NCT06887465


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Locations


Not yet recruiting

United States, Pennsylvania

Thomas Jefferson University

Philadelphia, Pennsylvania, United States, 19107

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