Early Prediction of Major Adverse Cardiovascular Events Using Remote Monitoring

Completed

Conditions studied: Ischemic Heart Disease

In brief

Usual care may not identify subtle clinical changes that precede a major adverse cardiovascular event (MACE). Therefore investigators will explore the effectiveness of using biomarkers, patient reported outcomes (PROs), and patient reported informatics (PRIs) as predictors to a MACE event.

Key facts

Study ID

NCT03064360

Run by

Cedars-Sinai Medical Center

People needed

200

Starts

2017-02-13

Expected to finish

2020-01-01

Last updated by the study team

2020-07-21

Who can join

Age: 18 and older, up to 105. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient age 18 years or older
• Patient with history of Ischemic Heart Disease
• Access to iOS or Android device
• Ambulatory

You may not qualify if…

• Patient with planned revascularization or valve surgery
• Patients with acute coronary syndrome
• Patients with psychiatric or substance abuse

Where it is running

• Cedars-Sinai Medical Center — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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