Status:
UNKNOWN
Establish a Telecare Model of Acute Coronary Syndrome Patient With Heart Stent Implantation by a Non-invasive Wearable Device and Artificial Intelligence Cloud to Reducing Medical Adverse Events.
Lead Sponsor:
Taipei Medical University Shuang Ho Hospital
Collaborating Sponsors:
Taipei Medical University WanFang Hospital
Taipei Medical University Hospital
Conditions:
Acute Coronary Syndrome
Percutaneous Transluminal Coronary Angioplasty
Eligibility:
All Genders
20+ years
Brief Summary
Heart disease is still one of the world's most important health problems, and it ranks second among the top ten causes of death among Taiwan. The main cause of death is acute coronary syndrome, and va...
Detailed Description
This study is open, prospective study, multi-center, randomized controlled trial, unobtrusive research. This study is start on June 1 2020. We will enroll 400 patients who diagnosis of acute coronary ...
Eligibility Criteria
Inclusion
- ≥ 20-year-old
- Patients performing general metal stent surgery
- Diagnosis of Acute Coronary Syndrome
- Willing to sign the consent form of the subject and cooperate with the return visit
- Those who are admitted to the hospital and enter the general ward can receive the first ECG heart sound examination
Exclusion
- \<20-year-old
- Before the stent was installed, the same blood vessel had been used in patients with PCI (percutaneous coronary intervention) and CABG (Coronary artery bypass graft).
- Those who cannot perform the first examination after being admitted to the hospital and entering the general ward
- It is impossible to measure the group of ECG and heart sounds. For example, when using Pacemaker, the ECG showed ventricular tachycardia (VT) and Dextrocardia on admission.
- Patients who are bedridden and have difficulty in cooperating with return visits
- Any subject that the physician believes is at high risk for future uncooperative tracking
- Direct participants in this program
Key Trial Info
Start Date :
July 20 2020
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
July 20 2024
Estimated Enrollment :
400 Patients enrolled
Trial Details
Trial ID
NCT04455568
Start Date
July 20 2020
End Date
July 20 2024
Last Update
July 23 2020
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