Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINOCA

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device, Diagnostic test
Study Type: Observational
SUMMARY

Myocardial infarction with non-obstructive coronary arteries (MINOCA) (i.e.\<50% stenoses) on coronary angiography) is an underappreciated clinical entity concerning 5-6% of patients with acute myocardial infarction. Approximately 50% of these patients remain without appropriate diagnosis and treatment. The MINOCA study aims at systematically assessing the frequency of underlying pathologies of MINOCA and outcomes with a multidisciplinary etiologic work-up and follow-up of 5 years including, for the first time, an implantable cardiac monitor (ICM) to assess the frequency of atrial fibrillation as underlying cause for MINOCA.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• ≥18 years of age

• Written informed consent

• Acute myocardial infarction (AMI) type 1 in accordance with the 4th universal definition of myocardial infarction

• Non-obstructive coronary arteries on angiography defined as the absence of coronary artery stenoses ≥50% in any potential infarct-related artery

• No clinically overt specific cause for the acute presentation

• Subendocardial or transmural late gadolinum enhancement (LGE) consistent with an ischemic etiology on cardiac magnetic resonance imaging (CMR)

• No clear underlying cause of MINOCA and therefore increased probability of atrial fibrillation

• ≥18 years of age

• Written informed consent

• AMI type 1 in accordance with the 4th universal definition of myocardial infarction

• Non-obstructive coronary arteries on angiography defined as the absence of coronary artery stenoses ≥50% in any potential infarct-related artery

• No clinically overt specific cause for the acute presentation

• Subendocardial or transmural LGE consistent with an ischemic etiology on CMR

Locations
Other Locations
Switzerland
Bern University Hospital Inselspital
RECRUITING
Bern
University Hospital Zurich USZ
RECRUITING
Zurich
Contact Information
Primary
Lorenz Räber, MD, PhD
lorenz.raeber@insel.ch
+41 31 632 50 00
Backup
Sarah Bär, MD
sarah.baer@insel.ch
Time Frame
Start Date: 2022-05-24
Estimated Completion Date: 2031-05-15
Participants
Target number of participants: 60
Treatments
ICM group
Patients eligible for ICM implantation for screening of atrial fibrillation
Non-ICM group
Patients ineligible for ICM implantation due to 1) refusal, 2) contraindication, or 3) clear underlying cause of MINOCA before ICM implantation.
Related Therapeutic Areas
Sponsors
Collaborators: Abbott, Bangerter-Rhyner Stiftung, University Hospital, Zürich
Leads: Insel Gruppe AG, University Hospital Bern

This content was sourced from clinicaltrials.gov