Arrhythmia Detection After Myocardial Infarction Trial

Status: Recruiting
Location: See location...
Intervention Type: Device, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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

• 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

• Willing to receive ICM insertion within 21 days of index AMI

Locations
United States
Pennsylvania
UPMC Presbyterian Hospital
RECRUITING
Pittsburgh
Contact Information
Primary
Samir F Saba, MD
sabas@upmc.edu
412 647 2695
Backup
Melissa Enlow
enlowms@upmc.edu
412-647-1582
Time Frame
Start Date: 2022-08-09
Estimated Completion Date: 2026-10-01
Participants
Target number of participants: 200
Treatments
Active_comparator: Control
Post-AMI patients in this arm will receive standard of care
Experimental: ICM
Post-AMI patients in this arm will receive standard of care and an ICM
Related Therapeutic Areas
Sponsors
Collaborators: Abbott
Leads: Samir Saba

This content was sourced from clinicaltrials.gov