Arrhythmia Detection After MI

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSamir Saba

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

Treatment groups

200 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Samir Saba

Lead sponsor

University of Pittsburgh

Sponsor institution

Abbott

Collaborator