Non-Invasive Blood Pressure Accuracy Study for Adult Subject Populations

Recruiting now · Not applicable

Conditions studied: Blood Pressure, Blood Pressure Measurement

In brief

The purpose of this study is to collect NIBP and invasive aortic pressure data from the clinical setting.

Key facts

Study ID

NCT07628296

Run by

GE Healthcare

People needed

130

Starts

2026-05-19

Expected to finish

2027-06-30

Last updated by the study team

2026-07-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age requirement: 18 and over.
• Have an upper limb (right OR left side) that fits the cuff size of the device (circumference ranging 17 cm to 40 cm) OR have a thigh (right OR left side) that fits a cuff size of the device (circumference ranging 38 to 50 cm).
• Have an arterial line as a standard of care, which measures blood pressure at the aortic root.
• Able to provide written informed consent.
• Expected to remain in the unit for the duration of the study procedure.

You may not qualify if…

• Have previously participated in this study (no subject may participate more than once).
• Pregnant and lactating women per site standard of care.
• Subjects with peripheral arterial diseases (causing left/right arm difference)
• Hemodynamically unstable subjects at the discretion of the investigator.
• Exhibited injuries, deformities, intravenous lines, or other abnormalities that, in the opinion of the Investigator, may prevent proper cuff application or functioning.
• Are suffering from infection(s) or immunocompromised patients that require isolation.
• PI or designee decision due to subject health conditions

Where it is running

• Tampere Heart Hospital — Tampere, Finland (enrolling)

Full record on ClinicalTrials.gov

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