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RECRUITINGOBSERVATIONAL

Wearable Devices Faciliate the Management of AMI Patients

Wearable Device for Characterizing AMI Patients After Primary PCI and Predicting the Clinical Outcomes

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The study will explore the use of wearable technology to consistently monitor patients with acute myocardial infarction (AMI) receiving primary percutaneous coronary intervention (PCI). Parameters such as heart rate, sleep time, physical activity, and blood pressure will be collected and analyzed to characterize the patients and predict clinical outcomes.

Who May Be Eligible (Plain English)

Who May Qualify: - Aged 18-75 years old - Diagnosed with STEMI or NSTEMI (ACC/AHA guidelines) - Half male and half female - Undergo CAG and PCI treatment; - Written willing to sign a consent form. Who Should NOT Join This Trial: - People under the age of 18 years old; - Patients who are pregnant/breastfeeding; - Patients who are allergic to the metallic or plastic components of the wearable devices Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Aged 18-75 years old * Diagnosed with STEMI or NSTEMI (ACC/AHA guidelines) * Half male and half female * Undergo CAG and PCI treatment; * Written informed consent. Exclusion Criteria: * People under the age of 18 years old; * Patients who are pregnant/breastfeeding; * Patients who are allergic to the metallic or plastic components of the wearable devices

Locations (1)

Renji Hospital
Shanghai, China