Surveillance Monitoring as an Alternative to Telemetry

Stopped early · Not applicable

Conditions studied: Telemetry, Patient Monitoring

In brief

The purpose of the study is to evaluate the impact of surveillance monitoring versus telemetry monitoring on clinical, healthcare economics, resource utilization, and qualitative outcomes.

Key facts

Study ID

NCT03039738

Run by

Medtronic - MITG

People needed

206

Starts

2017-04-03

Expected to finish

2018-01-04

Last updated by the study team

2019-05-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Signed and dated informed consent by subject
• Male or female 18 years of age or older
• Expected hospitalized admission on the general care floor or medical surgical unit for at least one overnight stay and/or > 12 hours
• Scheduled for telemetry monitoring
• Diagnosis indicates American Heart Association (AHA) telemetry Class III or none and therefore not indicated for telemetry monitoring
• For surveillance monitoring group subjects, treating provider who scheduled subject for telemetry agrees to alternative monitoring plan of surveillance monitoring
• Willingness to have study devices attached and hair shaved at sensor location as needed during study participation
• Willingness to participate in all aspects of the study

You may not qualify if…

• Implanted pacemaker or atrial defibrillator
• Allergy or sensitivity to ECG leads or adhesives that are similar to ECG leads
• Current AHA Class I or II indication/prescription for telemetry monitoring
• Prescription for other continuous condition monitoring such as capnography or pulse oximetry
• Ongoing opioid therapy by patient-controlled analgesia (PCA), by epidural or intrathecal infusions or by intravenous analgesia, per Investigator discretion
• Ventilated or intubated patients at the time of enrollment
• Female subject is pregnant, lactating, trying to get pregnant, or has a positive pregnancy test for women with childbearing potential
• Condition that, in the opinion of the investigator, may prevent completion of the study or protocol requirements
• Subject is considered as being morbidly obese (defined as BMI >50.0)

Where it is running

• Washington University in Saint Louis — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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