The HIgh-fidelity Hydraulic couPling Upper-arm Cuff Assessment of Limits, Safety, and Effectiveness (HIPULSE) Trial

Philips

Status

Enrolling

Conditions

Cardiac Surgery, Non-Cardiac ICU

Treatments

Device: Philips Advanced Monitoring Cuff (i.e. AMC)

Study type

Observational

Funder types

Industry

Identifiers

NCT06895590

BP FR_ AMC vs A-line and NIBP

Details and patient eligibility

About

The purpose of this study is to compare measurements of blood pressure (BP) and fluid responsiveness between the Philips AMC and invasive radial arterial line in surgical patients.

Full description

Primary Objective:

• To evaluate equivalence of BP measurements (Systolic Blood Pressure [SBP], Diastolic Blood Pressure [DBP], and Mean Arterial Pressure [MAP]) derived from the Philips AMC to the radial arterial line as ground truth.

Secondary Objectives:

To evaluate equivalence of Pulse Rate (PR) obtained by the Philips AMC to the radial arterial line as the ground truth.
To evaluate equivalence of Pulse Pressure Variation (PPV) obtained by the Philips AMC to calculated PPV obtained using the radial arterial line waveform pulse pressures as the ground truth.
To evaluate equivalence of Stroke Volume Variation (SVV) obtained by the Philips AMC to calculated SVV (e.g. from a predicate device that uses the radial arterial line waveform) as the ground truth.
To evaluate superiority of blood pressure measurements obtained by the Philips AMC to the oscillometric non-invasive blood pressure (NIBP) cuff, with the radial arterial line as the reference.
To evaluate trending agreement of BP and fluid responsiveness measurements.
To assess time to apply the Philips AMC relative to the radial arterial line.
To assess time from set-up start to first measurement completion between the Philips AMC and radial arterial line.
To collect and report safety data from the Philips AMC.
To collect and report system user experience and satisfaction scores from Philips AMC users.
To create a research dataset with the collected data to use for future hemodynamic algorithm development and validation.

Hypothesis: Blood pressure measurements derived from the Philips AMC are equivalent to the radial arterial line and superior to the oscillometric non-invasive blood pressure (NIBP) cuff.

Enrollment

205 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Adults aged 18 years and older
Indication for NIBP cuff
Indication for a radial arterial line
Subject or legal authorized representative is able to understand and speak the local language (also Spanish for US sites) to provide voluntary written informed consent prior to study procedures

The following stratification criteria must be met across the study sites and hence targeted enrollment may be required:

Age of every patient 18+; at least 30% > 65 years, 30% ≤ 65 years
At least 30% male, 30% female
Minimum number of subjects needed to test each size cuff (per ISO81060-2:2018/AMD2:2024, based on limb circumference range):
- Adult Small (19-27 cm) = 165*[8/(2*24)] = 28
- Adult (25-34 cm) = 165*[9/(2*24)] = 31
- Adult Large Short (30-40 cm with severely conical arm) = 165*[10/(2*24)] = 35
- Adult Large (32-43 cm) = 165*[11/(2*24)] = 38
At least 40% of the subjects within each cuff size shall have a limb circumference that lies within the upper half of the specified range of use of the cuff
At least 40% of the subjects within each cuff size shall have a limb circumference within the lower half of the specified range of use of the cuff
At least 10% SBP measurements ≤ 100 mmHg
At least 10% SBP measurements ≥ 160 mmHg
At least 10% DBP measurements ≤ 70 mmHg
At least 10% DBP measurements ≥ 85 mmHg

Exclusion criteria

Emergency surgery
Surgeries in which both arms are tucked
Inability to place the Philips AMC appropriately due to subject anatomy or condition
Known pregnancy or lactating women (self-report)
Patients treated with an intra-aortic balloon pump
Aortic and mitral regurgitation (> 2nd degree), if known
Measurements taken in the lateral position
Pressure of the arterial line system, when tested at 100 mmHg with the VeriCal device, exceeds the +/- 2 mmHg threshold
Currently participating in an investigational drug or another device study that clinically interferes with the study endpoints
Upper arm circumference < 19 cm or > 43 cm
BMI > 45
If the average of 3 baseline NIBP lateral difference measurements for SBP is > 15 mmHg or for DBP is > 10 mmHg
At the PI's discretion, subject does not qualify to participate in the study for any reasons that are not mentioned above