About this trial
Patients post acute myocardial infarction (AMI) have a high risk of mortality but the use of an implantable defibrillator in the early aftermath of an AMI has not been shown to improve patients' survival. The VEST trial recently demonstrated an improved overall survival in post AMI patients with the use of a wearable defibrillator. The same improvement was not demonstrated for the risk of sudden cardiac death. Monitoring patients after AMI using an implantable cardiac monitor (ICM) may document findings that can impact patient management and eventually improve their outcomes. We are therefore conducting the AID MI trial to examine the impact of ICM on patient management in the post AMI setting.
Eligibility criteria
Qualifiers
Adults, age 18 years or older
AMI (STEMI and NSTEMI)
Willing to give written informed consent
Expected discharge from hospital within 7 days of AMI
Disqualifiers
Existing pacemaker, ICD, ICM, or any other implantable cardiac electronic device
Pregnant
Index AMI was more than 21 days
Unwilling/cannot insert ICM within 21 days post AMI
Trial design
Treatments tested in this trial
- Standard of Care
- ICM Implantation