Tiered Inpatient Telemetry

Overview

About this study

The goal of this study is to support the development of a tiered inpatient cardiac telemetry program and leverage technologies to work toward the capability for all general care beds to have a plug-and-play cardiac monitoring.

The objective of this study is to test and validate InfoBionic inpatient telemetry technology. Patients will be simultaneously monitored using Philips and InfoBionic technology to compare service, technology and inform future build.

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:

Age 18+.
Capable of consenting.
Actively being monitored on Philips inpatient telemetry.

Exclusion Criteria:

Under the age of 18.
Unable to consent.
Pregnant patients.

Eligibility last updated 4/21/22. Questions regarding updates should be directed to the study team contact.

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	Contact
Rochester, Minn. Mayo Clinic principal investigator Peter Noseworthy, M.D., M.B.A.	Closed for enrollment	Contact information: Levi Disrud C.C.R.C. (507) 422-5241 Disrud.Levi@mayo.edu

Mayo Clinic Location

Status

Contact

Rochester, Minn.

Mayo Clinic principal investigator

Peter Noseworthy, M.D., M.B.A.

Closed for enrollment

Contact information:

Levi Disrud C.C.R.C.

(507) 422-5241

Disrud.Levi@mayo.edu

More information

Publications

Publications are currently not available

Clinical Trials