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

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
China
Renji Hospital
RECRUITING
Shanghai
Contact Information
Primary
Zhiguo Zou, MD, PhD
zouzhiguo@renji.com
+86 13524596108
Time Frame
Start Date: 2024-04-01
Estimated Completion Date: 2025-10-01
Participants
Target number of participants: 400
Sponsors
Leads: RenJi Hospital

This content was sourced from clinicaltrials.gov