Early Identification of Clinical Deterioration Using a Wearable Monitoring Device

  • STATUS
    Recruiting
  • participants needed
    1000
  • sponsor
    Biobeat Technologies Ltd.
Updated on 19 February 2024

Summary

This study aims to provide myriad of physiological parameters in patients admitted in an internal medicine department, and which are defined as being in an increased risk of clinical deterioration within the first 72-hours after admission. The investigators will also conduct a retrospective comparison between physiological changes in patients who did deteriorate to those who did not. This will form the basis for the development of an algorithm for early prediction and warning of physiological and clinical deterioration during the first 72-hours of admission.

Details
Condition Clinical Deterioration, Hemodynamic Instability
Age 18years - 99years
Treatment non-invasive monitoring
Clinical Study IdentifierNCT04220359
SponsorBiobeat Technologies Ltd.
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Males and females 18 years old and above admitted to the internal medicine department
On admission, the primary investigator assess their risk to deteriorate during the first 72 hours after admission as reasonably high
The patient is assigned to a "monitoring bed" within the department
The patient has signed an informed consent form

Exclusion Criteria

Lack of informed consent
It is known in advance that the patient cannot take part in the study for a 72-hours period (e.g. a patient that will be taken to surgery within the next 24 hours)
Technical inability to attach the Biobeat patch (BB-613PW) to the patients chest
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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