REducing 30-day ADMIssions in posT-discharge Subjects (READMIT)

Completed

Conditions studied: Acute Decompensated Heart Failure

In brief

The purpose of this observational study is to collect and characterize multiple physiologic data from a broad subset of subjects with acute heart failure (HF) Changes in physiologic data are expected to correlate with 30-day readmission rates in this population

Key facts

Study ID

NCT01574144

Run by

Medtronic Cardiac Rhythm and Heart Failure

People needed

70

Starts

2012-04-01

Expected to finish

2013-08-01

Last updated by the study team

2022-12-30

Who can join

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

You may qualify if…

• Subject with acute decompensated heart failure
• Subject (or legal guardian) willing to give consent for their participation
• Subject ≥18 years of age

You may not qualify if…

• Subject who is expected to receive a heart transplant or a ventricular assist device within 6 months
• Subject who cannot tolerate placement of external patch monitor on chest in the proposed location (ECG Lead II orientation)
• Subject with known allergies or hypersensitivities to adhesives or hydrogels
• Subject with implantable devices with active minute ventilation sensors.
• Subject who will not comply to study protocol requirements. This includes completing required data collection, and attending required follow up study visits.

Where it is running

• Scripps Green Hospital — La Jolla, California, United States
• Bay Area Cardiology — Tampa, Florida, United States
• United Heart and Cardiovascular — Saint Paul, Minnesota, United States
• Morristown Memorial Hospital — Morristown, New Jersey, United States
• Mohawk Valley Heart Institute — Utica, New York, United States
• University of Cincinnati — Cincinnati, Ohio, United States
• Vanderbilt University — Nashville, Tennessee, United States
• The Alfred Hospital — Melbourne, Victoria, Australia

Full record on ClinicalTrials.gov

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