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Evaluation and Calibration of a Novel Non-invasive Wearable Device for Monitoring Vital Signs

A Multi-center, Prospective, Pilot Study Intended for Data Collection to Evaluate and Calibrate a Novel Non-invasive Wearable Device for Monitoring Vital Signs

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04081987
Enrollment
50
Registered
2019-09-09
Start date
2019-11-20
Completion date
2020-03-31
Last updated
2020-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intensive Care Unit Patients, Post-cardiac Surgery

Keywords

Arterial line, Non-invasive monitoring, Vital signs, Blood pressure

Brief summary

The purpose of this clinical study is to compare the measurement of vital signs (blood pressure, heart rate, respiration rate, blood oxygen levels and body temperature) measured by the non-invasive, continuous and wireless BiPS monitoring device with vital signs measured by current standard of care hospital equipment (blood pressure measurements will be obtained from arterial line) an invasive arterial line. The study will be conducted in two medical centers in Israel and include 50 adult patients that are connected to an arterial line as part of their routine care.

Detailed description

BiPS Medical has developed a wearable, wireless device that conveniently monitors important vital sign trends over time - blood pressure (diastolic & systolic), heart and respiration rates, blood oxygen level (SPO2) and body temperature - to aid in identifying clinical deterioration. The device is base on a combination of inflatable mini finger cuff and photoplethysmograph technology. The aim of this study is to collect data for evaluating and calibrating of the BiPS monitor for monitoring patient vital signs and compare it to current standard of care hospital monitors. The study population includes a total of 50 adult patients that are connected to an arterial line as part of their routine care. The BiPS non-invasive monitor will be attached to participating patients during their stay in the ICU/ recovery in cardiac ICU/Post Anesthesia Care Unit /other hospital designated unit. The device will be placed on the patient for 60 minutes while in hospital bed, in which up to 20 blood pressure measurements are performed (each takes up to 60 seconds). Heart and respiration rates, body temperature and SPO2 will be measured continuously while the device is attached to the patient hand.

Interventions

Comparing blood pressure (diastolic & systolic), heart and respiration rates, blood oxygen level and body temperature measurement using the BiPS non-invasive monitor to an arterial line.

Sponsors

Tel-Aviv Sourasky Medical Center
CollaboratorOTHER_GOV
Carmel Medical Center
CollaboratorOTHER
BiPS Medical
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged 18 years and older who agree to sign an informed consent. * Patients connected to an arterial line as part of their routine care (e.g., patients recovering from cardiac or other major surgery)

Exclusion criteria

* Pregnant women. * Patients under the age of 18. * Patients who are not connected to an arterial line as part of their routine care. * Unable to give informed consent. * Patients with poor or no finger pulse.

Design outcomes

Primary

MeasureTime frameDescription
Level of accordance between the BiPS monitor and the arterial line60 minutesCorrelation between the vital sgns measured on The BiPS non-invasive monitor and those measured through the arterial line

Countries

Israel

Contacts

Primary ContactTomer Zaidenberg
tomer@bipsmedical.com+972-52-2793242

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026