Heart Failure Study to Evaluate Vital Signs and Overcome Low Use of Guideline-Directed Therapy by Remote Monitoring

Stopped early · Not applicable

Conditions studied: Heart Failure

In brief

A study evaluating the impact of remotely collected data, measured using digital technologies, on the use of guideline-recommended heart failure therapy in adult participants with heart failure.

Key facts

Study ID

NCT04292275

Run by

Amgen

People needed

18

Starts

2020-03-06

Expected to finish

2021-10-01

Last updated by the study team

2023-08-08

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• History of chronic heart failure.
• Ejection fraction equal to or below 40%.
• New York Heart Association (NYHA) class II to class III.
• Enrollment during or within 30 days after a hospitalization, emergency department, or urgent, unscheduled clinic/office visit with primary diagnosis of heart failure.

You may not qualify if…

• Has received a major organ transplant (e.g., lung, liver, heart, bone marrow, kidney).
• Currently in an investigational device or drug study.
• Unwilling or unable to wear a digital wrist watch device for measuring blood pressure and other parameters during waking hours.

Where it is running

• Yale New Haven Hospital — New Haven, Connecticut, United States
• Cardiology Associates of Fairfield County, PC — Stamford, Connecticut, United States
• MercyOne Northeast Iowa Family Medicine and Residency — Waterloo, Iowa, United States
• Virtua Health Inc. — Voorhees Township, New Jersey, United States
• Duke University Medical Center — Durham, North Carolina, United States
• Diagnostic Cardiology Group — Chattanooga, Tennessee, United States
• Tennessee Center for Clinical Trials, a division of Cardiology and Vascular Associates PLLC — Tullahoma, Tennessee, United States
• Inova Heart and Vascular Institute — Falls Church, Virginia, United States

Full record on ClinicalTrials.gov

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