A Study of Wearable Wireless Device in Addition to Standard Monitoring to Record Vital Signs in Patients in the ICU/Stepdown Unit

Overview

About this study

The purpose of the study is to validate wearable device monitoring with standard ICU/stepdown patient vital signs monitoring especially heart rate, telemetry, respiratory rate, blood pressure, and pulse oximetry.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

18 years or over with unselected acute medical or surgical diagnosis admitted to the stepdown/ICU
Patients deemed to need continuous vital signs monitoring in the ICU/step-down

Exclusion Criteria:

Postoperative cardiac surgery patients
Postoperative transplant surgery patients
Patient refusal to participate in the study
Patient agitation and unable to consent or participate in the study
Attending physician on clinical service indicates that patient is not a candidate for the study

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status
Scottsdale/Phoenix, Ariz. Mayo Clinic principal investigator Ayan Sen, M.D.	Closed for enrollment

Mayo Clinic Location

Status

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Ayan Sen, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

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