Philips Non-Invasive Blood Pressure Validation Study of VS30 Monitor

NCT ID: NCT06980766

Last Updated: 2025-12-09

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 99 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2025-03-10
• Study Completion Date: 2025-03-31

Brief Summary

The purpose of this study is to provide supporting documentation of the blood pressure performance for the Philips EarlyVue VS30 monitor on the intended adult and pediatric population. The same arm sequential method with dual observer auscultation will be used to collect data.

Detailed Description

The Philips EarlyVue VS30 monitor, and approved Philips Gentle Care cuffs will be evaluated in comparison to dual reference auscultation. The study will consist of a minimum of 85 participants, specifically, 35 children aged 3-12 years and 50 participants older than 12 years. The participants enrolled will approximate the distribution of blood pressures and biceps circumferences as outlined in ISO 81060-2:2018/AMD 2:2024. The maximum number of participants enrolled will not exceed 170 participants.

Blood pressure measurements will follow ISO 81060-2:2018/AMD 2:2024, Section 5.2.4.1 Same arm sequential method.

Two trained observers, typically a Registered Nurse (RN), Licensed Practical Nurse (LPN), or Respiratory Therapist (RT) will observe (listen to) the Korotkoff sounds at the artery at the site of cuff placement. The reference blood pressure measurements observed by the auscultators will be performed sequentially with the device under test. The auscultators will complete 1 or 2 initial baseline auscultatory reference blood pressure measurements and device under test measurements. This is followed by 3 to 8 paired blood pressure readings of auscultatory reference blood pressure measurements alternated with device under test measurements. All participants must contribute 3 valid paired data points requiring three DUT readings paired with three reference blood pressure readings. The reference blood pressure readings for analysis will be the average of the reference dual auscultation values before and after DUT reading.

The data included for the final analysis will contain no fewer than 35 participants aged 3-12 years, and no fewer than 50 participants over the age of 12 and a minimum of 255 valid paired observations.

Conditions

Non Invasive Blood Pressure

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Pediatrics Participants aged 3-12 years

Device: Non-invasive blood pressure Manual blood pressure via sphygmomanometer

Or

Non invasive blood pressure via EarlyVue VS30 Monitor

Non Invasive Blood Pressure

Intervention Type: DEVICE

Manual blood pressure via sphygmomanometer

Or

Non invasive blood pressure via earlyvue VS30 Monitor

Adults Participants aged 12-85 years

Device: Non-invasive blood pressure Manual blood pressure via sphygmomanometer

Or

Non invasive blood pressure via EarlyVue VS30 Monitor

Non Invasive Blood Pressure

Intervention Type: DEVICE

Manual blood pressure via sphygmomanometer

Or

Non invasive blood pressure via earlyvue VS30 Monitor

Interventions

Non Invasive Blood Pressure

Manual blood pressure via sphygmomanometer

Or

Non invasive blood pressure via earlyvue VS30 Monitor

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Participants must be able to provide an informed consent or have legally authorized representative consent to participate.
• Participants that are between 7 and 17 years of age must provide assent to participate in the study.
• Participant must be willing and able to comply with the study procedures.
• Participant or legally authorized representative must be able to read or write in English.
• Participant must be 3 to 85 years of age.
• Participants must have an arm circumference in the range of 14-45 centimeters.

Exclusion Criteria

• Participant is unwilling to provide informed consent.
• Participants with deformities or abnormalities that may prevent proper application of the device under test.
• Participants whose upper arm circumference is less than 14 cm or greater than 45 cm.
• Female participants who are self-reported as pregnant, or who are self-reported as trying to get pregnant.
• Participants with known heart arrhythmias.
• Participants with peripheral vascular disease.
• Participants with clotting disorders.
• History of bleeding disorders or personal history of prolonged bleeding from injury
• History of blood clots
• Hemophilia
• Participants that cannot tolerate sitting for up to 1 hour.
• Participant with a blood pressure demographic that has already been filled.
• Other known health conditions that will prevent safe participation in the study upon disclosure in health assessment form or verbally.
• Participant is evaluated by the investigator or clinician and found to be medically unsuitable for participation in this study.

• Minimum Eligible Age: 3 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Element Materials Technology

INDUSTRY

Sponsor Role: collaborator

Philips Clinical & Medical Affairs Global

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Monica Rabanal, NP

Role: PRINCIPAL_INVESTIGATOR

Element

Locations

Element Materials Technology

Louisville, Colorado, United States

Countries

United States

Other Identifiers

PR2024-610_CC-2024-300840

Identifier Type: -

Identifier Source: org_study_id