RecruitingNot ApplicableNCT05073419

Arrhythmia Detection After MI

Arrhythmia Detection After Myocardial Infarction Trial


Sponsor

Samir Saba

Enrollment

200 participants

Start Date

Aug 9, 2022

Study Type

INTERVENTIONAL

Conditions

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

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called ICM Implantation and Standard of Care for people with acute myocardial infarction. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERStandard of Care

Routine monitoring of post AMI patient with clinic visits

DEVICEICM Implantation

Implantation of ICM through small incision (2 mm) under the skin


Locations(1)

UPMC Presbyterian Hospital

Pittsburgh, Pennsylvania, United States

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NCT05073419


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