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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03382990
Other study ID # Stent-AF Trial
Secondary ID
Status Not yet recruiting
Phase N/A
First received December 19, 2017
Last updated December 19, 2017
Start date January 1, 2018
Est. completion date December 31, 2019

Study information

Verified date December 2017
Source Mackay Memorial Hospital
Contact Chao-Feng Lin, MD
Phone +886-2-2543-3535
Email thcpci@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The benefit of a drug-eluting stent (DES) in patients with acute myocardial infarction (AMI) is controversial. This study will aim to observe the effect of a DES on the risk of new-onset AF in patients with AMI.


Description:

Acute myocardial infarction (AMI) is the leading cause of mortality in the world. Early invasive strategy with percutaneous coronary intervention (PCI) has been demonstrated to be the most effective strategy to treat AMI. Although drug-eluting stent (DES) has not shown benefits to reduce mortality rate among AMI patients compared with bare-metal stent (BMS), the use of DES in real-world is increasing because of reduced restenosis rates. AMI patients are at higher risk to develop atrial fibrillation (AF) than general population. However, whether early PCI with DES implantation is related to a reduced risk of AF still remains unclear. The purpose of this study is to investigate the association of DES implantation and the risk of AF among patients with AMI treated by early PCI.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40000
Est. completion date December 31, 2019
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Patients were enrolled by primary diagnostic coding as acute myocardial infarction and treatment coding as receiving PCI between 2007 and 2013 in Taiwan National Health Insurance Research Database (NHIRD)

Exclusion Criteria:

1. Less than 20-years-old; Unknown sex and age

2. Not residents in Taiwan

3. Died during AMI admission

4. Previous history of AF

5. Receiving coronary artery bypass grafting (CABG), ventricular assist device (VAD), extracorporeal membrane oxygenation (ECMO), and heart transplantation during observational and/or database period

6. No stent implantation during PCI

7. Unknown stent types

Study Design


Intervention

Device:
DES or BMS
DES or BMS placement during the procedure of PCI in patients with AMI is depend on the operator's decision.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Mackay Memorial Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary new-onset atrial fibrillation new record or diagnostic claims of atrial fibrillation after hospital discharge from acute myocardial infarction one year
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